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1.
Phytother Res ; 36(10): 3900-3910, 2022 Oct.
Article in English | MEDLINE | ID: mdl-36104304

ABSTRACT

Heilaohu, the roots of Kadsura coccinea, has been used in Tujia ethnomedicine to treat rheumatic arthritis (RA). Heilaohuacid G (1), a new 3,4-seco-lanostane type triterpenoid isolated from the ethanol extract of Heilaohu, whose structure was determined using HR-ESI-MS data, NMR spectroscopic analyses, and ECD calculations. In this study, our purpose is to elucidate the mechanisms of Heilaohuacid G in the treatment of RA by inhibited proliferation of rheumatoid arthritis-fibroblastoid synovial (RA-FLS) cells and inhibited the inflammatory reactions in LPS-induced RA-FLS and RAW 264.7 cell lines via inhibiting NF-κB pathway. The biological activity screening experiments indicated that Heilaohuacid G significantly inhibited proliferation of RA-FLS cells with IC50 value of 8.16 ± 0.47 µM. CCK-8 assay, ELISA, flow cytometry assay, and Western blot were used to measure the changes of cell viability, apoptosis, and the release of inflammatory cytokines. Heilaohuacid G was found not only induced RA-FLS cell apoptosis, but also inhibited the inflammatory reactions in LPS-induced RA-FLS and RAW 264.7 cell lines via inhibiting NF-κB pathway. Furthermore, Heilaohuacid G (p.o.) at doses of 3.0, 6.0, and 12.0 mg/kg and the ethanol extracts of Heilaohu (p.o.) at doses of 200, 400, and 800 mg/kg both were confirmed antiinflammatory effects on xylene-induced ear mice edema model.


Subject(s)
Arthritis, Rheumatoid , Kadsura , Osteoarthritis , Rheumatic Fever , Triterpenes , Animals , Apoptosis , Arthritis, Rheumatoid/drug therapy , Arthritis, Rheumatoid/metabolism , Cell Proliferation , Cells, Cultured , Cytokines/metabolism , Ethanol/pharmacology , Fibroblasts/metabolism , Inflammation/drug therapy , Inflammation/metabolism , Lipopolysaccharides/pharmacology , Mice , NF-kappa B/metabolism , Plant Extracts/therapeutic use , RAW 264.7 Cells , Rheumatic Fever/metabolism , Synovial Membrane , Triterpenes/pharmacology , Triterpenes/therapeutic use , Xylenes/metabolism , Xylenes/pharmacology , Xylenes/therapeutic use
2.
Cochrane Database Syst Rev ; 6: CD007462, 2020 06 25.
Article in English | MEDLINE | ID: mdl-32580252

ABSTRACT

BACKGROUND: The risk of maternal mortality and morbidity is higher after caesarean section than for vaginal birth. With increasing rates of caesarean section, it is important to minimise risks to the mother as much as possible. This review focused on different skin preparations to prevent infection. This is an update of a review last published in 2018. OBJECTIVES: To compare the effects of different antiseptic agents, different methods of application, or different forms of antiseptic used for preoperative skin preparation for preventing postcaesarean infection. SEARCH METHODS: For this update, we searched Cochrane Pregnancy and Childbirth's Trials Register, ClinicalTrials.gov, the WHO International Clinical Trials Registry Platform (ICTRP) (9 July 2019), and reference lists of retrieved studies. SELECTION CRITERIA: Randomised and quasi-randomised trials, evaluating any type of preoperative skin preparation (agents, methods or forms). We included studies presented only as abstracts, if there was enough information to assess risk of bias. Comparisons of interest in this review were between: different antiseptic agents (e.g. alcohol, povidone iodine), different methods of antiseptic application (e.g. scrub, paint, drape), different forms of antiseptic (e.g. powder, liquid), and also between different packages of skin preparation including a mix of agents and methods, such as a plastic incisional drape, which may or may not be impregnated with antiseptic agents. We mainly focused on the comparison between different agents, with and without the use of drapes. Only studies involving the preparation of the incision area were included. This review did not cover studies of preoperative handwashing by the surgical team or preoperative bathing. DATA COLLECTION AND ANALYSIS: Three review authors independently assessed all potential studies for inclusion, assessed risk of bias, extracted the data and checked data for accuracy. We assessed the certainty of the evidence using the GRADE approach. MAIN RESULTS: We included 13 individually-randomised controlled trials (RCTs), with a total of 6938 women who were undergoing caesarean section. Twelve trials (6916 women) contributed data to this review. The trial dates ranged from 1983 to 2016. Six trials were conducted in the USA, and the remainder in India, Egypt, Nigeria, South Africa, France, Denmark, and Indonesia. The included studies were broadly at low risk of bias for most domains, although high risk of detection bias raised some specific concerns in a number of studies. Length of stay was only reported in one comparison. Antiseptic agents Parachlorometaxylenol with iodine versus iodine alone We are uncertain whether parachlorometaxylenol with iodine made any difference to the incidence of surgical site infection (risk ratio (RR) 0.33, 95% confidence interval (CI) 0.04 to 2.99; 1 trial, 50 women), or endometritis (RR 0.88, 95% CI 0.56 to 1.38; 1 trial, 50 women) when compared with iodine alone, because the certainty of the evidence was very low. Adverse events (maternal or neonatal) were not reported. Chlorhexidine gluconate versus povidone iodine Moderate-certainty evidence suggested that chlorhexidine gluconate, when compared with povidone iodine, probably slightly reduces the incidence of surgical site infection (RR 0.72, 95% CI 0.58 to 0.91; 8 trials, 4323 women). This effect was still present in a sensitivity analysis after removing four trials at high risk of bias for outcome assessment (RR 0.87, 95% CI 0.62 to 1.23; 4 trials, 2037 women). Low-certainty evidence indicated that chlorhexidine gluconate, when compared with povidone iodine, may make little or no difference to the incidence of endometritis (RR 0.95, 95% CI 0.49 to 1.86; 3 trials, 2484 women). It is uncertain whether chlorhexidine gluconate reduces maternal skin irritation or allergic skin reaction (RR 0.64, 95% CI 0.28 to 1.46; 3 trials, 1926 women; very low certainty evidence). One small study (60 women) reported reduced bacterial growth at 18 hours after caesarean section for women who had chlorhexidine gluconate preparation compared with women who had povidone iodine preparation (RR 0.23, 95% CI 0.07 to 0.70). Methods Drape versus no drape This comparison investigated the use of drape versus no drape, following preparation of the skin with antiseptics. Low-certainty evidence suggested that using a drape before surgery compared with no drape, may make little or no difference to the incidence of surgical site infection (RR 1.29, 95% confidence interval (CI) 0.97 to 1.71; 3 trials, 1373 women), and probably makes little or no difference to the length of stay in the hospital (mean difference (MD) 0.10 days, 95% CI -0.27 to 0.46; 1 trial, 603 women; moderate-certainty evidence). One trial compared an alcohol scrub and iodophor drape with a five-minute iodophor scrub only, and reported no surgical site infection in either group (79 women, very-low certainty evidence). We were uncertain whether the combination of a one-minute alcohol scrub and a drape reduced the incidence of metritis when compared with a five-minute scrub, because the certainty of the evidence was very low (RR 1.62, 95% CI 0.29 to 9.16; 1 trial, 79 women). The studies did not report on adverse events (maternal or neonatal). AUTHORS' CONCLUSIONS: Moderate-certainty evidence suggests that preparing the skin with chlorhexidine gluconate before caesarean section is probably slightly more effective at reducing the incidence of surgical site infection in comparison to povidone iodine. For other outcomes examined there was insufficient evidence available from the included RCTs. Most of the evidence in this review was deemed to be very low or low certainty. This means that for most findings, our confidence in any evidence of an intervention effect is limited, and indicates the need for more high-quality research. Therefore, it is not yet clear what sort of skin preparation may be most effective for preventing postcaesarean surgical site infection, or for reducing other undesirable outcomes for mother and baby. Well-designed RCTs, with larger sample sizes are needed. High-priority questions include comparing types of antiseptic (especially iodine versus chlorhexidine), and application methods (scrubbing, swabbing, or draping). We found two studies that are ongoing; we will incorporate the results of these studies in future updates of this review.


Subject(s)
Anti-Infective Agents, Local/therapeutic use , Cesarean Section/adverse effects , Endometritis/prevention & control , Preoperative Care/methods , Surgical Drapes , Surgical Wound Infection/prevention & control , Adult , Anti-Infective Agents, Local/adverse effects , Bandages , Chlorhexidine/adverse effects , Chlorhexidine/analogs & derivatives , Chlorhexidine/therapeutic use , Endometritis/epidemiology , Ethanol/therapeutic use , Female , Humans , Iodine/therapeutic use , Iodophors/therapeutic use , Length of Stay , Povidone-Iodine/adverse effects , Povidone-Iodine/therapeutic use , Pregnancy , Randomized Controlled Trials as Topic , Surgical Wound Infection/epidemiology , Xylenes/therapeutic use
3.
Cochrane Database Syst Rev ; 10: CD007462, 2018 10 22.
Article in English | MEDLINE | ID: mdl-30346040

ABSTRACT

BACKGROUND: The risk of maternal mortality and morbidity (particularly postoperative infection) is higher for caesarean section (CS) than for vaginal birth. With the increasing rate of CS, it is important to minimise the risks to the mother as much as possible. This review focused on different forms and methods of preoperative skin preparation to prevent infection. This review is an update of a review that was first published in 2012, and updated in 2014. OBJECTIVES: To compare the effects of different antiseptic agents, different methods of application, or different forms of antiseptic used for preoperative skin preparation for preventing postcaesarean infection. SEARCH METHODS: For this update, we searched Cochrane Pregnancy and Childbirth's Trials Register, ClinicalTrials.gov, the WHO International Clinical Trials Registry Platform (ICTRP) (27 November 2017), and reference lists of retrieved studies. SELECTION CRITERIA: Randomised and quasi-randomised trials, evaluating any type of preoperative skin preparation agents, forms, and methods of application for caesarean section.Comparisons of interest in this review were between different antiseptic agents used for CS skin preparation (e.g. alcohol, povidone iodine), different methods of antiseptic application (e.g. scrub, paint, drape), different forms of antiseptic (e.g. powder, liquid), and also between different skin preparations, such as a plastic incisional drape, which may or may not be impregnated with antiseptic agents.Only studies involving the preparation of the incision area were included. This review did not cover studies of preoperative handwashing by the surgical team or preoperative bathing. DATA COLLECTION AND ANALYSIS: Three review authors independently assessed all potential studies for inclusion, assessed risk of bias, and extracted the data using a predesigned form. We checked data for accuracy. We assessed the quality of the evidence using the GRADE approach. MAIN RESULTS: For this update, we included 11 randomised controlled trials (RCTs), with a total of 6237 women who were undergoing CS. Ten trials (6215 women) contributed data to this review. All included studies were individual RCTs. We did not identify any quasi- or cluster-RCTs. The trial dates ranged from 1983 to 2016. Six trials were conducted in the USA, and the remainder in Nigeria, South Africa, France, Denmark, and Indonesia.The included studies were broadly methodologically sound, but raised some specific concerns regarding risk of bias in a number of cases.Drape versus no drapeThis comparison investigated the use of a non-impregnated drape versus no drape, following preparation of the skin with antiseptics. For women undergoing CS, low-quality evidence suggested that using a drape before surgery compared with no drape, may make little or no difference to the incidence of surgical site infection (risk ratio (RR) 1.29, 95% confidence interval (CI) 0.97 to 1.71; 2 trials, 1294 women), or length of stay in the hospital (mean difference (MD) 0.10 day, 95% CI -0.27 to 0.46 1 trial, 603 women).One-minute alcohol scrub with iodophor drape versus five-minute iodophor scrub without drapeOne trial compared an alcohol scrub and iodophor drape with a five-minute iodophor scrub only, and reported no surgical site infection in either group (79 women, very-low quality evidence). We were uncertain whether the combination of a one-minute alcohol scrub and a drape reduced the incidence of endomyometritis when compared with a five-minute scrub, because the quality of the evidence was very low (RR 1.62, 95% CI 0.29 to 9.16; 1 trial, 79 women).Parachlorometaxylenol with iodine versus iodine aloneWe were uncertain whether parachlorometaxylenol with iodine before CS made any difference to the incidence of surgical site infection (RR 0.33, 95% CI 0.04 to 2.99; 1 trial, 50 women), or endometritis (RR 0.88, 95% CI 0.56 to 1.38; 1 trial, 50 women) when compared with iodine alone, because the quality of the evidence was very low.Chlorhexidine gluconate versus povidone iodineLow-quality evidence suggested that chlorhexidine gluconate before CS, when compared with povidone iodine, may make little or no difference to the incidence of surgical site infection (RR 0.80, 95% CI 0.62 to 1.02; 6 trials, 3607 women). However, surgical site infection appeared to be slightly reduced for women for whom chlorhexidine gluconate was used compared with povidone iodine after we removed four trials at high risk of bias for outcome assessment, in a sensitivity analysis (RR 0.59, 95% CI 0.37 to 0.95; 2 trials, 1321 women).Low-quality evidence indicated that chlorhexidine gluconate before CS, when compared with povidone iodine, may make little or no difference to the incidence of endometritis (RR 1.01, 95% CI 0.51 to 2.01; 2 trials, 2079 women), or to reducing maternal skin irritation or allergic skin reaction (RR 0.60, 95% CI 0.22 to 1.63; 2 trials, 1521 women).One small study (60 women) reported reduced bacterial growth at 18 hours after CS for women who had chlorhexidine gluconate preparation compared with women who had povidone iodine preparation (RR 0.23, 95% CI 0.07 to 0.70).None of the included trials reported on maternal mortality or repeat surgery.Chlorhexidine 0.5% versus 70% alcohol plus drapeOne trial, which was only available as an abstract, investigated the effect of skin preparation on neonatal adverse events, and found cord blood iodine concentration to be higher in the iodine group. AUTHORS' CONCLUSIONS: There was insufficient evidence available from the included RCTs to fully evaluate different agents and methods of skin preparation for preventing infection following caesarean section. Therefore, it is not yet clear what sort of skin preparation may be most effective for preventing postcaesarean surgical site infection, or for reducing other undesirable outcomes for mother and baby.Most of the evidence in this review was deemed to be very low or low quality. This means that for most findings, our confidence in any evidence of an intervention effect is limited, and indicates the need for more high-quality research.This field needs high quality, well designed RCTs, with larger sample sizes. High priority questions include comparing types of antiseptic (especially iodine versus chlorhexidine), and application methods (scrubbing, swabbing, or draping). We found four studies that were ongoing; we will incorporate the results of these studies in future updates of this review.


Subject(s)
Anti-Infective Agents, Local/therapeutic use , Cesarean Section/adverse effects , Endometritis/prevention & control , Surgical Wound Infection/prevention & control , Adult , Bandages , Chlorhexidine/therapeutic use , Ethanol/therapeutic use , Female , Humans , Iodine/therapeutic use , Iodophors/therapeutic use , Length of Stay , Povidone-Iodine/therapeutic use , Pregnancy , Preoperative Care/methods , Randomized Controlled Trials as Topic , Surgical Drapes , Xylenes/therapeutic use
4.
BMC Complement Altern Med ; 16(1): 511, 2016 Dec 08.
Article in English | MEDLINE | ID: mdl-27931220

ABSTRACT

BACKGROUND: Musk is widely used in clinical practice for its anti-cancer properties. Here, we treated various types of cancer using musk to determine which cancers are sensitive to musk treatment. We also compared effects of native musk and synthetic musk ketone in cancer cells. Furthermore, we investigated mechanisms underlying effects of musk. METHODS: Twenty two cancer cell lines were treated with musk. Cell proliferation and apoptosis analyses were carried out. Native musk and synthetic musk ketone were analyzed by gas chromatograph-mass spectrometer (GC-MS) assay. Differentially expressed genes were determined by microarray and quantitative real-time polymerase chain reaction. RESULTS: Native musk strongly induced the growth repression and the apoptosis in the majority of cancer cell lines in a dose-dependent manner, but distinct types of cancer showed significantly different reactions. Cancer cells which originated from epithelial cells showed higher sensitivity for musk treatment. By contrast, leukaemia and lymphoma cells were not sensitive. GC-MS analysis demonstrated that native musk contains more than 30 contents in which musk ketone is a major component; synthetic musk ketone was consistent with natural musk ketone, and the used sample of synthetic musk ketone contained only sole component. Similar to native musk, synthetic musk ketone induced the growth repression and the apoptosis of cancer cells. Additionally, numerous genes were differentially expressed in lung cancer cells after native musk treatment. These differentially expressed genes were involved in many signalling pathways. Among these pathways, apoptosis-related pathways included interleukin family, tumor necrosis factor family, and MAPK signalling pathway. Native musk and synthetic musk ketone can up-regulate IL-24 (interleukin family) and DDIT3 (MAPK signalling pathway) in lung cancer cells. CONCLUSIONS: This research provided strong evidence that native musk and synthetic musk ketone can induce the growth repression and the apoptosis of cancer cells. However, the selection of sensitive cancer patient for individualized treatment is a key step in clinical application. Synthetic musk ketone can substitute for native musk to treat cancer patients. Musk might induce the growth repression and the apoptosis of lung cancer cells through up-regulating IL-24 and DDIT3 expressions.


Subject(s)
Apoptosis/drug effects , Cell Proliferation/drug effects , Fatty Acids, Monounsaturated/therapeutic use , Lung Neoplasms/drug therapy , Xylenes/therapeutic use , Cell Line, Tumor , Drug Screening Assays, Antitumor , Fatty Acids, Monounsaturated/pharmacology , Gas Chromatography-Mass Spectrometry , Humans , Signal Transduction , Xylenes/pharmacology
5.
Biosens Bioelectron ; 67: 450-7, 2015 May 15.
Article in English | MEDLINE | ID: mdl-25256782

ABSTRACT

Implantable neural prosthetics devices offer a promising opportunity for the restoration of lost functions in patients affected by brain or spinal cord injury, by providing the brain with a non-muscular channel able to link machines to the nervous system. Nevertheless current neural microelectrodes suffer from high initial impedance and low charge-transfer capacity because of their small-feature geometry (Abidian et al., 2010; Cui and Zhou, 2007). In this work we have developed PEDOT-modified neural probes based on flexible substrate capable to answer to the three critical requirements for neuroprosthetic device: efficiency, lifetime and biocompatibility. We propose a simple procedure for the fabrication of neural electrodes fully made of Parylene-C, followed by an electropolymerization of the active area with the conductive polymer PEDOT that is shown to greatly enhance the electrical performances of the device. In addition, the biocompatibility and the very high SNR exhibited during signal recording make our device suitable for long-term implantation.


Subject(s)
Biosensing Techniques , Brain/physiopathology , Coated Materials, Biocompatible/therapeutic use , Brain/drug effects , Coated Materials, Biocompatible/chemistry , Electrodes, Implanted , Humans , Neurons/drug effects , Neurons/physiology , Polymers/chemistry , Polymers/therapeutic use , Xylenes/chemistry , Xylenes/therapeutic use
6.
Cochrane Database Syst Rev ; (9): CD007462, 2014 Sep 17.
Article in English | MEDLINE | ID: mdl-25229700

ABSTRACT

BACKGROUND: The risk of maternal mortality and morbidity (particularly postoperative infection) is higher for caesarean section than for vaginal birth. With the increasing rate of caesarean section, it is important that the risks to the mother are minimised as far as possible. This review focuses on different forms and methods for preoperative skin preparation to prevent infection. OBJECTIVES: To compare the effects of different agent forms and methods of preoperative skin preparation for preventing postcaesarean infection. SEARCH METHODS: We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (26 June 2014) and the reference lists of all included studies and review articles. SELECTION CRITERIA: Randomised and quasi-randomised trials, including cluster-randomised trials, evaluating any type of preoperative skin preparation agents, forms and methods of application for caesarean section. DATA COLLECTION AND ANALYSIS: Three review authors independently assessed all potential studies for inclusion, assessed risk of bias and extracted the data using a predesigned form. Data were checked for accuracy. MAIN RESULTS: We included six trials with a total of 1522 women. No difference was found in the primary outcomes of either wound infection or endometritis. Two trials of 1294 women, compared drape with no drape (one trial using iodine and the other using chlorhexidine) and found no significant difference in wound infection (risk ratio (RR) 1.29; 95% confidence interval (CI) 0.97 to 1.71). One trial of 79 women comparing alcohol scrub and iodophor drape with iodophor scrub without drape reported no wound infection in either group. One trial of 50 women comparing parachlorometaxylenol plus iodine with iodine alone reported no significant difference in wound infection (RR 0.33; 95% CI 0.04 to 2.99).Two trials reported endometritis, one trial comparing alcohol scrub and iodophor drape with iodophor scrub only found no significant difference (RR 1.62; 95% CI 0.29 to 9.16). The other trial of 50 women comparing parachlorometaxylenol plus iodine with iodine alone reported no significant difference in endometritis (RR 0.88; 95% CI 0.56 to 1.38). One trial of 60 women comparing chlorhexidine gluconate with povidone-iodine reported significant lower rates of bacterial growth at 18 hours after caesarean section (RR 0.23, 95% CI 0.07 to 0.70). No difference was found in the secondary outcome of either length of stay or reduction of skin bacteria colony count. No trial reported other maternal outcomes, i.e. maternal mortality, repeat surgery and re-admission resulting from infection. One trial, which was only available as an abstract, investigated the effect of skin preparation on neonatal adverse events and found cord blood iodine concentration to be significantly higher in the iodine group.Most of the risk of bias in the included studies was unclear in selection bias and attrition bias. The quality of the evidence using GRADE was low for wound infection comparing drape versus no drape, one-minute alcohol scrub with iodophor drape versus five-minute iodophor scrub without drape, and parachlorometaxylenol with iodine versus iodine alone. The quality of the evidence for wound infection comparing chlorhexidine gluconate with povidone-iodine was very low. AUTHORS' CONCLUSIONS: This review found that chlorhexidine gluconate compared with iodine alone was associated with lower rates of bacterial growth at 18 hours after caesarean section. However, this outcome was judged as very low quality of evidence. Little evidence is available from the included randomised controlled trials to evaluate different agent forms, concentrations and methods of skin preparation for preventing infection following caesarean section. Therefore, it is not yet clear what sort of skin preparation may be most efficient for preventing postcaesarean wound and surgical site infection.There is a need for high-quality, properly designed randomised controlled trials with larger sample sizes in this field. High priority questions include comparing types of antiseptic (especially iodine versus chlorhexidine), the timing and duration of applying the antiseptic (especially previous night versus day of surgery, and application methods (scrubbing, swabbing and draping).


Subject(s)
Anti-Infective Agents, Local/therapeutic use , Cesarean Section/adverse effects , Endometritis/prevention & control , Surgical Wound Infection/prevention & control , Adult , Bandages , Chlorhexidine/therapeutic use , Ethanol/therapeutic use , Female , Humans , Iodine/therapeutic use , Iodophors/therapeutic use , Pregnancy , Randomized Controlled Trials as Topic , Xylenes/therapeutic use
7.
Cochrane Database Syst Rev ; (9): CD007462, 2012 Sep 12.
Article in English | MEDLINE | ID: mdl-22972109

ABSTRACT

BACKGROUND: The risk of maternal mortality and morbidity (particularly postoperative infection) is higher for caesarean section than for vaginal birth. With the increase in caesarean section, it is important that the risks to the mother are minimised as far as possible. This review focuses on different forms and methods for preoperative skin preparation to prevent infection. OBJECTIVES: To compare the effects of different agent forms and methods of preoperative skin preparation for preventing postcaesarean infection. SEARCH METHODS: We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (2 January 2012) and the reference lists of all included studies and review articles SELECTION CRITERIA: Randomised and quasi-randomised trials, including cluster-randomised trials, evaluating any type of preoperative skin preparation agents, forms and methods of application for caesarean section. DATA COLLECTION AND ANALYSIS: Three review authors independently assessed all potential studies for inclusion, assessed risk of bias and extracted the data using a predesigned form. Data were checked for accuracy. MAIN RESULTS: We included five trials with a total of 1462 women. No difference was found in the primary outcomes of either wound infection or endometritis. Two trials of 1294 women, compared drape with no drape (one trial using iodine and the other using chlorhexidine) and found no significant difference in wound infection (risk ratio (RR) 1.29; 95% confidence interval (CI) 0.97 to 1.71). One trial of 79 women comparing alcohol scrub and iodophor drape with iodophor scrub without drape reported no wound infection in either group. One trial of 50 women comparing parachlorometaxylenol plus iodine with iodine alone reported no significant difference in wound infection (RR 0.33; 95% CI 0.04 to 2.99).Two trials reported endometritis, one trial comparing alcohol scrub and iodophor drape with iodophor scrub only found no significant difference (RR 1.62; 95% CI 0.29 to 9.16). The other trial of 50 women comparing parachlorometaxylenol plus iodine with iodine alone reported no significant difference in endometritis (RR 0.88; 95% CI 0.56 to 1.38). No difference was found in the secondary outcome of either length of stay or reduction of skin bacteria colony count. No trial reported other maternal outcomes, i.e. maternal mortality, repeat surgery and re-admission resulting from infection. One trial, which was only available as an abstract, investigated the effect of skin preparation on neonatal adverse events and found cord blood iodine concentration to be significantly higher in the iodine group. AUTHORS' CONCLUSIONS: Little evidence is available from the included randomised controlled trials to evaluate different agent forms, concentrations and methods of skin preparation for preventing infection following caesarean section. Therefore, it is not yet clear what sort of skin preparation may be most efficient for preventing postcaesarean wound and surgical site infection. There is a need for high-quality, properly designed randomised controlled trials with larger sample sizes in this field. High priority questions include comparing types of antiseptic (especially iodine versus chlorhexidine), the timing and duration of applying the antiseptic (especially previous night versus day of surgery, and application methods (scrubbing, swabbing and draping).


Subject(s)
Anti-Infective Agents, Local/therapeutic use , Cesarean Section/adverse effects , Endometritis/prevention & control , Surgical Wound Infection/prevention & control , Adult , Bandages , Chlorhexidine/therapeutic use , Ethanol/therapeutic use , Female , Humans , Iodine/therapeutic use , Iodophors/therapeutic use , Pregnancy , Randomized Controlled Trials as Topic , Xylenes/therapeutic use
8.
Article in English | MEDLINE | ID: mdl-20955955

ABSTRACT

OBJECTIVE: The aim of this study was to compare GPX instruments and hand files for gutta-percha removal. STUDY DESIGN: Fifty maxillary central incisors with a single straight canal were instrumented and filled. The teeth were divided into 5 groups of 10 specimens each, according to the gutta-percha removal techniques: group 1: GPX (21-mm-long teeth); group 2: GPX and xylol as solvent (21-mm-long teeth); group 3: GPX (25-mm-long teeth); group 4: GPX and xylol as solvent (25-mm-long teeth); and group 5: hand files and xylol as solvent. The amount of time for gutta-percha removal and the number of fractured instruments were evaluated. Radiographs were taken, and the teeth were grooved longitudinally and split. The area of residual debris was measured using Sigma Scan software. RESULTS: The time for filling material removal was significantly shorter when GPX was used (P < .05). Overall, hand files and solvent produced fewer remnants of filling materials (P < .05). In the GPX 25 mm-long teeth group, the filling material was not removed in the apical third. CONCLUSIONS: Under the experimental conditions, the GPX instruments proved to be faster than hand instruments in removing root filling materials; however, hand instruments left a smaller amount of residual filling materials on the canal walls. The GPX instruments did not pull the gutta-percha beyond its tip.


Subject(s)
Dental Pulp Cavity/pathology , Gutta-Percha/chemistry , Root Canal Filling Materials/chemistry , Root Canal Preparation/instrumentation , Solvents/therapeutic use , Dental Alloys/chemistry , Dentin/pathology , Equipment Design , Equipment Failure , Humans , Materials Testing , Retreatment , Root Canal Obturation , Stainless Steel/chemistry , Time Factors , Tooth Apex/pathology , Xylenes/therapeutic use , Zinc Oxide-Eugenol Cement/therapeutic use
9.
Pharmacology ; 86(2): 65-72, 2010.
Article in English | MEDLINE | ID: mdl-20639685

ABSTRACT

BACKGROUND/AIM: To discover new 5-lipoxygenase (5-LO) inhibitors applicable to inflammation-related skin disease, we identified and examined antiinflammatory properties of a novel 5-LO inhibitor, KR-33749, in vitro and in vivo. METHODS: 5-LO enzyme activity was assayed using insect cell lysates overexpressing rat 5-LO. The leukotriene B(4) (LTB(4)) level was assayed in rat basophilic leukemia (RBL-1) cell line. Mouse ear edema was induced by topical application of arachidonic acid. Atopic dermatitis-like skin lesion was induced by topical application of 1-chloro-2,4-dinitrobenzene (DNCB) to NC/Nga mice. RESULTS: KR-33749 inhibited 5-LO activity with an IC(50) value of 70.5 +/- 6.0 nmol/l in parallel with LTB(4) inhibition in RBL-1 cells. The compound exhibited a >1,000-fold selectivity against 12-LO and 15-LO. KR-33749 showed in vivo protective effects against arachidonic acid-induced ear edema and DNCB-induced atopic dermatitis-like symptoms in NC/Nga mice. CONCLUSION: Our results show that KR-33749, a new 5-LO inhibitor exhibits potent antiinflammatory activities in vitro as well as in vivo.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Arachidonate 5-Lipoxygenase/metabolism , Lipoxygenase Inhibitors/pharmacology , Lipoxygenase Inhibitors/therapeutic use , Thiazoles/pharmacology , Thiazoles/therapeutic use , Xylenes/pharmacology , Xylenes/therapeutic use , Animals , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Arachidonate 5-Lipoxygenase/genetics , Arachidonic Acid/toxicity , Cell Line, Tumor , Dermatitis, Atopic/drug therapy , Dermatitis, Atopic/immunology , Dermatitis, Atopic/pathology , Dinitrochlorobenzene/toxicity , Dose-Response Relationship, Drug , Edema/prevention & control , Isoenzymes/antagonists & inhibitors , Leukotriene B4/metabolism , Lipoxygenase Inhibitors/administration & dosage , Male , Mice , Mice, Inbred BALB C , Osmolar Concentration , Rats , Recombinant Proteins/antagonists & inhibitors , Skin/drug effects , Skin/pathology , Skin Diseases/drug therapy , Thiazoles/administration & dosage , Time Factors , Xylenes/administration & dosage
10.
Plast Surg Nurs ; 27(4): 185-9; quiz 190-1, 2007.
Article in English | MEDLINE | ID: mdl-18165724

ABSTRACT

Pre-operative skin preparation of the surgical site using appropriate anti-septic product is recognized by the Centers for Disease Control and Prevention Guideline for Prevention of Surgical Site Infection, 1999, as a strongly recommended intervention to prevent surgical site infection. This article reviews anti-septic surgical skin preparation products according to the Food and Drug Administration classifications, efficacy, and safety. It also examines pertinent research regarding anti-septic products. This information provides the peri-operative registered nurse with information to make appropriate decisions when choosing anti-septic skin preparation products for surgical patients.


Subject(s)
Anti-Infective Agents, Local/therapeutic use , Preoperative Care/methods , Skin Care/methods , 2-Propanol/therapeutic use , Administration, Cutaneous , Anti-Infective Agents, Local/adverse effects , Anti-Infective Agents, Local/classification , Asepsis/methods , Asepsis/standards , Chlorhexidine/analogs & derivatives , Chlorhexidine/therapeutic use , Drug Combinations , Humans , Infection Control/methods , Infection Control/standards , Iodophors/therapeutic use , Patient Selection , Perioperative Nursing , Povidone-Iodine/therapeutic use , Practice Guidelines as Topic , Preoperative Care/nursing , Preoperative Care/standards , Safety , Skin Care/nursing , Skin Care/standards , Surgical Wound Infection/epidemiology , Surgical Wound Infection/etiology , Surgical Wound Infection/prevention & control , Treatment Outcome , United States/epidemiology , United States Food and Drug Administration , Xylenes/therapeutic use
11.
Drugs Exp Clin Res ; 29(3): 101-5, 2003.
Article in English | MEDLINE | ID: mdl-14708455

ABSTRACT

A 12-week double-blind randomized study was performed to compare benzoyl peroxide 5% (BP) gel and chloroxylenol 0.5% plus salicylic acid 2% (PCMX + SA) cream (Nisal cream) for efficacy and adverse reactions. Thirty-seven volunteers participated in the study, 19 in the BP group and 18 in the PCMX + SA group. The patients applied the medication twice daily to the entire face. Clinical evaluation and lesion counts were obtained at 0, 3, 6, 9 and 12 weeks. At week 12 both groups showed a marked improvement in both inflammatory and noninflammatory lesions (60% and 54% for the BP group and 62% and 56% for and 56% for the PCMX + SA group, respectively). Although PCMX + SA showed a slightly stronger keratolytic effect throughout the study period, there was no statistically significant difference in the reduction of the papulopustules or comedones between the two groups. Adverse effects such as erythema and photosensitivity were significantly fewer in the PCMX + SA group at week 12 (p = 0.0002 and p = 0.05, respectively). These results suggest that PCMX + SA cream is as effective as BP gel in the treatment of papulopustular and comedonal acne and that it is better tolerated.


Subject(s)
Acne Vulgaris/drug therapy , Benzoyl Peroxide/therapeutic use , Facial Dermatoses/drug therapy , Gels , Ointments , Salicylic Acid/therapeutic use , Xylenes/therapeutic use , Administration, Topical , Adolescent , Adult , Benzoyl Peroxide/administration & dosage , Benzoyl Peroxide/adverse effects , Double-Blind Method , Drug Administration Schedule , Drug Combinations , Drug Synergism , Female , Humans , Male , Propionibacterium acnes/drug effects , Salicylic Acid/administration & dosage , Salicylic Acid/pharmacology , Staphylococcus aureus/drug effects , Treatment Outcome , Xylenes/administration & dosage , Xylenes/pharmacology
12.
Am J Dent ; 14(4): 233-7, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11699743

ABSTRACT

PURPOSE: To investigate the antimicrobial efficacy of a chlorhexidine gluconate (2.0%) and of an ethanolic chloroxylenol solution (10%) as a temporary root canal dressing against selected test microorganisms (Staphylococcus aureus, Streptococcus faecium, Escherichia coli, Candida albicans). MATERIALS AND METHODS: Extracted single-rooted human teeth were instrumented up to size 40. After removal of the smear layer suspensions of the test microorganisms were inserted into the root canals. After incubation for 48 hrs each suspension of the test organisms was removed and the root canals were filled with one of the two different disinfectants. The teeth were then incubated for 48 hrs. Twelve teeth and three controls were used for each of the four test organisms and each of the two regimens. After incubation, each root canal was instrumented and the removed canal wall dentin was examined microbiologically. RESULTS: With a contact time of 48 hrs between the two disinfectants and the four bacterial suspensions the medications led to a total killing of microorganisms in 82% of a total of 96 contaminated teeth. In the dentin layer situated 50 microm from the root canal, both medications achieved bacterial killing in a range from 99.9% to 99.99%, depending on the test organism. There were no significant differences (P> 0.1) between the relative antimicrobial activity of the two root canal dressings.


Subject(s)
Anti-Infective Agents, Local/therapeutic use , Chlorhexidine/therapeutic use , Dental Pulp Diseases/drug therapy , Root Canal Irrigants/therapeutic use , Xylenes/therapeutic use , Anti-Infective Agents, Local/pharmacology , Candida albicans/drug effects , Chlorhexidine/pharmacology , Colony Count, Microbial , Dental Pulp Cavity/microbiology , Dental Pulp Diseases/microbiology , Dentin/microbiology , Enterococcus faecium/drug effects , Escherichia coli/drug effects , Humans , Infections/drug therapy , Microbial Sensitivity Tests , Root Canal Irrigants/pharmacology , Staphylococcus aureus/drug effects , Xylenes/pharmacology
13.
Surg Infect (Larchmt) ; 1(2): 109-14, 2000.
Article in English | MEDLINE | ID: mdl-12594898

ABSTRACT

OBJECTIVE: To determine outcome of infected surgical wounds treated with 3% para-chloro-meta-xylenol + 3% phospholipid PTC [PCMX-PL] (Techni-Care). DESIGN: Retrospective review of patient records. SETTING: University hospital. PATIENTS: Thirty consecutively treated patients (sixteen male, fourteen female) who had developed open infected wounds (twenty-one abdominal [seventy percent], nine extremity [thirty percent]). Mean patient age was 50.1 years. All wounds were treated with commonly practiced wound care techniques (e.g., debridement, frequent dressing changes using saline or topical antibiotics, and, in most cases, parenteral antibiotics) for an extended period of time prior to intervention (mean = 35 days). INTERVENTIONS: PCMX-PL, a topical microbicide, was used as adjunctive therapy. Eight outcome parameters were analyzed: (1) patient morbidity and mortality; (2) wound healing; (3) number of debridements; (4) wound culture results; (5) leukocytosis (peripheral white blood cell count > 10,000 cells/microl); (6) number of febrile days (temperature > 101 degrees F); (7) length of hospital stay; and (8) number of days of intensive care. RESULTS: No treatment failures or adverse reactions to PCMX-PL were seen. Twenty (sixty-seven percent) wounds were healed or had been successfully closed while ten (thirty-three percent) were granulating well at sixty-day follow-up. The number of debridements, positive wound cultures, white-blood-cells, and febrile days decreased after PCMX-PL treatment began. CONCLUSIONS: Despite severe underlying diseases, all patients were discharged from the hospital with closed or healing wounds. We recommend treatment with PCMX-PL as an adjunctive therapy for infected wounds particularly when standard care measures have failed.


Subject(s)
Anti-Infective Agents, Local/therapeutic use , Phospholipids/therapeutic use , Surgical Wound Infection/drug therapy , Wound Healing/drug effects , Xylenes/therapeutic use , Adult , Aged , Anti-Infective Agents, Local/pharmacology , Drug Combinations , Female , Humans , Male , Middle Aged , Phospholipids/pharmacology , Retrospective Studies , Salvage Therapy/methods , Treatment Outcome , Xylenes/pharmacology
14.
J Endod ; 25(8): 547-51, 1999 Aug.
Article in English | MEDLINE | ID: mdl-10635219

ABSTRACT

During and after chemomechanical preparation, particularly before the definitive filling of an infected root canal, a temporary intracanal dressing with an antimicrobial activity is generally indicated. Therefore, the aim of this study was to investigate the antimicrobial effect of ED 84, a liquid root canal disinfectant containing chloroxylenol (10%) and camphor (15%), against selected test organisms (Staphylococcus aureus, Streptococcus faecalis, Escherichia coli, and Candida albicans) both in vitro and under clinical conditions, using extracted teeth. With a contact time of 180 min between undiluted ED 84 and the four bacterial suspensions in the canal, there was a 2 to 3 log reduction in the number of organisms. Under in vitro conditions, the reduction was even greater than 3 logs. When using a liquid medication as a temporary root canal dressing for a duration of approximately 2 days, ED 84 can definitely be used.


Subject(s)
Anti-Infective Agents, Local/pharmacology , Camphor/pharmacology , Chlorophenols/pharmacology , Root Canal Irrigants/pharmacology , Anti-Infective Agents, Local/therapeutic use , Bacterial Infections/drug therapy , Camphor/therapeutic use , Candida albicans/drug effects , Chlorophenols/therapeutic use , Colony Count, Microbial , Dental Pulp Cavity/microbiology , Enterococcus faecalis/drug effects , Escherichia coli/drug effects , Humans , Root Canal Irrigants/therapeutic use , Staphylococcus aureus/drug effects , Xylenes/chemistry , Xylenes/pharmacology , Xylenes/therapeutic use
15.
J Bone Joint Surg Am ; 80(9): 1336-40, 1998 Sep.
Article in English | MEDLINE | ID: mdl-9759819

ABSTRACT

The coating of medical devices with antimicrobial agents has recently emerged as a potentially effective method for the prevention of device-related infections. We examined the anti-infective efficacy of intramedullary nails coated with an antiseptic combination of chlorhexidine and chloroxylenol in a rabbit model of device-related infection after fixation of an open tibial fracture. The rabbits were randomized to receive 2.8-by-100-millimeter stainless-steel tibial intramedullary nails that either were uncoated or were coated with antiseptic. After administration of anesthesia and preoperative antibiotic prophylaxis, a tibial fracture was created and then reduced with insertion of the intramedullary nail. A bacterial inoculum of 10(6) colony-forming units of Staphylococcus aureus was injected into the intramedullary canal, and the wound was sutured. Radiographs of the tibiae were made postoperatively, and the rabbits were monitored daily. They were killed at six weeks, or earlier if there was dehiscence of the wound, the fracture became grossly unstable, or the rabbit failed to thrive. The use of the antiseptic-coated nails was associated with a significantly lower rate of device-related osteomyelitis (two of twenty-two; 9 per cent) than the use of the uncoated nails (thirteen of twenty-one; 62 per cent) (p = 0.0003). The radiographic and histopathological findings were generally similar in the two groups of rabbits. Antiseptic agents were not detected in serum. The results suggest that antiseptic-coated fracture-fixation devices provide significant local protection against Staphylococcus aureus, which is the most common cause of infections related to orthopaedic devices.


Subject(s)
Anti-Infective Agents, Local/administration & dosage , Bone Nails , Chlorhexidine/administration & dosage , Fracture Fixation, Intramedullary , Premedication , Staphylococcal Infections/prevention & control , Tibial Fractures/surgery , Xylenes/administration & dosage , Animals , Anti-Infective Agents, Local/therapeutic use , Chlorhexidine/therapeutic use , Disease Models, Animal , Drug Therapy, Combination , Evaluation Studies as Topic , Rabbits , Random Allocation , Treatment Outcome , Xylenes/therapeutic use
16.
Med Parazitol (Mosk) ; (3): 42-5, 1996.
Article in Russian | MEDLINE | ID: mdl-9036283

ABSTRACT

Agents and biologically active fractions derived from medical plants grown in Siberia were tested in vitro and in vivo. The extract from the aspen bark displayed the highest antiopisthorchiatic activity. This agent given at a concentration of 10(-3) caused 100% death of Opisthorchis 72 hours later. In golden hamster experiments, the efficiency of the aspen bark extract was 73.48-83.0%. Butanolic and ethylacetatic extracts were found to have the greatest antiopisthorchiatic activity. The results of chemical and chromatographic studies indicated that active fractions contained salicine and its derivatives. The aspen bark extract produces no substantial toxic effect on laboratory animals and belongs to the class "Low-toxic substances".


Subject(s)
Antiplatyhelmintic Agents/therapeutic use , Trees , Animals , Antiplatyhelmintic Agents/pharmacology , Antiplatyhelmintic Agents/toxicity , Cricetinae , Drug Evaluation, Preclinical , Lethal Dose 50 , Male , Mesocricetus , Mice , Opisthorchiasis/drug therapy , Opisthorchiasis/parasitology , Opisthorchis/drug effects , Plant Extracts/pharmacology , Plant Extracts/therapeutic use , Plant Extracts/toxicity , Praziquantel/analogs & derivatives , Praziquantel/therapeutic use , Rats , Siberia , Time Factors , Xylenes/therapeutic use
17.
Cutis ; 53(6): 313-6, 1994 Jun.
Article in English | MEDLINE | ID: mdl-8070287

ABSTRACT

Onychomycosis is one of the most common causes of nail disease and one of the hardest to treat among fungal infections. A double-blind, vehicle-controlled study has been conducted to evaluate the safety and efficacy of Fungoid Tincture (Pedinol Pharmacal, Inc), for the treatment of fungal infection of the toenails. Ten patients with distal subungual onychomycosis were treated for twelve months with topical Fungoid Tincture. Another ten patients with the same ailment were treated with the vehicle alone. Once a month, clinical and global evaluation of the target nail was done, in addition to trimming and debridement of the nails. After twelve months of treatment, 90 percent of patients applying Fungoid Tincture showed negative results on culture. There were minimal adverse effects.


Subject(s)
Antifungal Agents/therapeutic use , Benzalkonium Compounds/therapeutic use , Cetylpyridinium/analogs & derivatives , Foot Dermatoses/drug therapy , Foot Dermatoses/microbiology , Onychomycosis/drug therapy , Propionates/therapeutic use , Triacetin/therapeutic use , Xylenes/therapeutic use , Administration, Cutaneous , Adolescent , Adult , Aged , Antifungal Agents/administration & dosage , Antifungal Agents/adverse effects , Benzalkonium Compounds/administration & dosage , Benzalkonium Compounds/adverse effects , Cetylpyridinium/administration & dosage , Cetylpyridinium/adverse effects , Cetylpyridinium/therapeutic use , Double-Blind Method , Drug Combinations , Female , Humans , Male , Middle Aged , Pharmaceutical Vehicles , Propionates/administration & dosage , Propionates/adverse effects , Safety , Toes , Triacetin/administration & dosage , Triacetin/adverse effects , Xylenes/administration & dosage , Xylenes/adverse effects
18.
Med Parazitol (Mosk) ; (2): 19-21, 1994.
Article in Russian | MEDLINE | ID: mdl-7935182

ABSTRACT

The paper deals with follow-ups of 4 patients with chronic opisthorchiasis, two of whom were treated with chloxylum and two with bilthricide. Eight-thirty six months after discontinuation of anthelmintics, there were recurrent or enhanced complaints, repeated finding of Opisthorchis eggs and antigens in the feces. These changes were accompanied by elevated blood eosinophil counts. It is suggested that Opisthorchis metacercariae can be long preserved in latency in the definitive host and recurrent opisthorchiasis forms may develop.


Subject(s)
Opisthorchiasis/diagnosis , Adult , Antiplatyhelmintic Agents/therapeutic use , Child , Chronic Disease , Female , Humans , Opisthorchiasis/drug therapy , Opisthorchiasis/parasitology , Praziquantel/therapeutic use , Recurrence , Time Factors , Xylenes/therapeutic use
19.
Med Parazitol (Mosk) ; (1): 23-6, 1994.
Article in Russian | MEDLINE | ID: mdl-8015517

ABSTRACT

The effects of chloxyl and praziquantel on the lipid phase of erythrocytic membranes and the antioxidative system were studied in 77 patients with opisthorchiasis. After chloxyl treatment, patients with chronic opisthorchiasis had significantly higher contents of dienic conjugates, malonic dialdehyde, Schiff bases; in blood plasma, alpha-tocopherol content had a tendency to decrease. Treatment with praziquantel caused an increase in the content of malonic dialdehyde only in the erythrocytic membrane. Ten-day preadministration of vitamin E in a dose of 2 mg/kg body weight reduced the pro-oxidative action of praziquantel.


Subject(s)
Anthelmintics/therapeutic use , Antioxidants , Erythrocyte Membrane/drug effects , Membrane Lipids/blood , Opisthorchiasis/drug therapy , Praziquantel/therapeutic use , Xylenes/therapeutic use , Acute Disease , Adolescent , Adult , Chronic Disease , Drug Therapy, Combination , Erythrocyte Membrane/metabolism , Female , Humans , Lipid Peroxidation/drug effects , Male , Opisthorchiasis/blood , Vitamin E/therapeutic use
20.
Med Parazitol (Mosk) ; (5): 6-13, 1993.
Article in Russian | MEDLINE | ID: mdl-8127275

ABSTRACT

About a 20-years period of chloxyl (hexaparaxylol) mass treatment of opisthorchiasis in hyper- and mesoendemic territories of Russia did not change the prevalence of the infection, reducing only by some degree its intensity. Morbidity and incapacity in treated patients and in cured ones paradoxically appeared to be higher than in untreated persons. High parasitocidal activity of praziquantel in trematode infections has tempted (20) to use the drug as a tool in improving the level of health of population of endemic areas. For areas with a moderate and with a high rates of the infection "radical" and "selective" treatment with praziquantel was proposed (6). The study of clinical and immunological parameters in aboriginal, settler and migrant population of hyperendemic area in the Ob-Irtysh basin--Khanty-Mansi Autonomous District revealed striking differences in the groups and their different responses to praziquantel treatment. The possibility of transplacental transmission of O. felineus antigens in aborigines and in a part of settlers leading to immunological tolerance was revealed. "Retreatment" with praziquantel can lead to the loss of the latter and can challenge higher morbidity in adults and unsafety of their progeny. Monitoring system, checking the results of "retreatment" with praziquantel is proposed.


Subject(s)
Opisthorchiasis/drug therapy , Praziquantel/therapeutic use , Adult , Antiplatyhelmintic Agents/therapeutic use , Child , Chronic Disease , Disease Reservoirs , Drug Monitoring , Drug Tolerance , Humans , Immune Tolerance , Native Hawaiian or Other Pacific Islander , Opisthorchiasis/ethnology , Opisthorchiasis/immunology , Racial Groups , Siberia , World Health Organization , Xylenes/therapeutic use
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