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1.
AAPS PharmSciTech ; 20(5): 198, 2019 May 24.
Article in English | MEDLINE | ID: mdl-31127389

ABSTRACT

In this work, several normal, oil-in-water (o/w) microemulsions (MEs) were prepared using peppermint essential oil, jojoba oil, trans-anethole, and vitamin E as oil phases to test their capacity to load paclitaxel (PTX). Initially, pseudo-ternary partial phase diagrams were constructed in order to find the normal microemulsion region using d-α-tocopherol polyethylene glycol 1000 succinate (TPGS-1000) as surfactant and isobutanol (iso-BuOH) as co-surfactant. Selected ME formulations were loaded with PTX reaching concentrations of 0.6 mg mL-1 for the peppermint oil and trans-anethole MEs, while for the vitamin E and jojoba oil MEs, the maximum concentration was 0.3 mg mL-1. The PTX-loaded MEs were stable according to the results of heating-cooling cycles and mechanical force (centrifugation) test. Particularly, drug release profile for the PTX-loaded peppermint oil ME (MEPP) showed that ∼ 90% of drug was released in the first 48 h. Also, MEPP formulation showed 70% and 90% viability reduction on human cervical cancer (HeLa) cells after 24 and 48 h of exposure, respectively. In addition, HeLa cell apoptosis was confirmed by measuring caspase activity and DNA fragmentation. Results showed that the MEPP sample presented a major pro-apoptotic capability by comparing with the unloaded PTX ME sample.


Subject(s)
Antineoplastic Agents, Phytogenic/chemical synthesis , Apoptosis/drug effects , Cytotoxins/chemical synthesis , Nanospheres/chemistry , Paclitaxel/chemical synthesis , Plant Oils/chemical synthesis , Antineoplastic Agents, Phytogenic/pharmacokinetics , Apoptosis/physiology , Cell Survival/drug effects , Cell Survival/physiology , Cytotoxins/pharmacokinetics , Dose-Response Relationship, Drug , Drug Liberation , HeLa Cells , Humans , Mentha piperita , Paclitaxel/pharmacokinetics , Plant Oils/pharmacokinetics , Polyethylene Glycols/chemical synthesis , Polyethylene Glycols/pharmacokinetics , Surface-Active Agents/chemical synthesis , Surface-Active Agents/pharmacokinetics , Vitamin E/chemical synthesis , Vitamin E/pharmacokinetics
2.
Braz Dent J ; 27(2): 208-16, 2016.
Article in English | MEDLINE | ID: mdl-27058386

ABSTRACT

The aim of this study was to evaluate the effect of concentration, exposure time and temperature of sodium hypochlorite (NaOCl) added with surfactants on its penetration into dentinal tubules. Sixty-five extracted human permanent maxillary anterior teeth with single canals were prepared by ProTaper SX hand-operated instruments. The teeth were then sectioned perpendicular to the long axis. The crowns and apical thirds of all the teeth were removed. The remaining roots were processed into 4-mm-long blocks and stained overnight in crystal violet. One hundred and thirty stained blocks were further split into halves and treated by nine different types of NaOCl-based solutions. Three solutions were added with surfactants (Hypoclean, H6, Chlor-Xtra) and the others were regular hypochlorites at increasing concentrations (1%, 2%, 4%, 5.25%, <6%, 6% NaOCl) from different brands. The dentin blocks were exposed to the solutions for 2, 5, and 20 min at 20 °C, 37 °C and 45 °C, respectively. The depth of NaOCl penetration was determined by bleaching of the stain and measured by light microscopy at 20x and 40x. Statistical comparisons were made by using a generalized linear model with Bonferroni's post-hoc correction. The shortest penetration (81±6.6 µm) was obtained after incubation in 1% NaOCl for 2 min at 20 °C; the highest penetration (376.3±3.8 µm) was obtained with Chlor-Xtra for 20 min at 45 °C. Varying NaOCl concentration produced a minimal effect while temperature and exposure time had a significant direct relationship with NaOCl penetration into dentinal tubules, especially those with lowered surface tension. The exposure time and temperature of sodium hypochlorite as well as the addition of surfactants may influence the penetration depth of irrigants into dentinal tubules.


Subject(s)
Dental Pulp Cavity/chemistry , Dentin/chemistry , Sodium Hypochlorite/chemistry , Surface-Active Agents/pharmacokinetics , Humans , Surface-Active Agents/chemistry
3.
Braz. dent. j ; Braz. dent. j;27(2): 208-216, Mar.-Apr. 2016. tab, graf
Article in English | LILACS | ID: lil-778335

ABSTRACT

Abstract The aim of this study was to evaluate the effect of concentration, exposure time and temperature of sodium hypochlorite (NaOCl) added with surfactants on its penetration into dentinal tubules. Sixty-five extracted human permanent maxillary anterior teeth with single canals were prepared by ProTaper SX hand-operated instruments. The teeth were then sectioned perpendicular to the long axis. The crowns and apical thirds of all the teeth were removed. The remaining roots were processed into 4-mm-long blocks and stained overnight in crystal violet. One hundred and thirty stained blocks were further split into halves and treated by nine different types of NaOCl-based solutions. Three solutions were added with surfactants (Hypoclean, H6, Chlor-Xtra) and the others were regular hypochlorites at increasing concentrations (1%, 2%, 4%, 5.25%, <6%, 6% NaOCl) from different brands. The dentin blocks were exposed to the solutions for 2, 5, and 20 min at 20 °C, 37 °C and 45 °C, respectively. The depth of NaOCl penetration was determined by bleaching of the stain and measured by light microscopy at 20 and 40. Statistical comparisons were made by using a generalized linear model with Bonferroni's post-hoc correction. The shortest penetration (81±6.6 μm) was obtained after incubation in 1% NaOCl for 2 min at 20 °C; the highest penetration (376.3±3.8 μm) was obtained with Chlor-Xtra for 20 min at 45 °C. Varying NaOCl concentration produced a minimal effect while temperature and exposure time had a significant direct relationship with NaOCl penetration into dentinal tubules, especially those with lowered surface tension. The exposure time and temperature of sodium hypochlorite as well as the addition of surfactants may influence the penetration depth of irrigants into dentinal tubules.


Resumo O objetivo deste estudo foi avaliar o efeito da concentração, tempo de exposição e temperatura de hipoclorito de sódio (NaOCl) acrescidos de tensioativos na penetração nos túbulos dentinários. Sessenta e cinco dentes superiores humanos uniradiculares extraídos foram preparadas usando instrumentos ProTaper SX operados manualmente. Os dentes foram seccionados perpendicularmente ao longo eixo. As coroas e o terço apical foram removidos. Os restantes das raízes foram transformadas em blocos de 4-mm de comprimento e coradas durante em violeta de cristal. Cento e trinta blocos foram posteriormente divididos em metades e tratados por nove tipos diferentes de soluções de NaOCl. Três soluções com tensioativos foram adicionadas (Hypoclean, H6, Chlor-Xtra); e os outros foram os hipocloritos regulares em concentrações crescentes (1, 2, 4, 5,25, <6 and 6% de NaOCl) de diferentes origens. Os blocos de dentina foram expostos às soluções de 2, 5 e 20 min a 20 °C, 37 °C e 45 °C, respectivamente. A profundidade de penetração do NaOCl foi determinada pelo branqueamento da mancha e medido em microscopia de luz com ampliações de 20× e 40×. Comparações estatísticas foram feitas usando um modelo linear generalizado com a correção de Bonferroni (post-hoc). A menor penetração (81±6,6 m) foi medida após incubação com 1% de hipoclorito de sódio durante 2 min a 20 °C; a maior penetração (376,3±3,8 m) foi obtida com Chlor-Xtra durante 20 min a 45 °C. Variando a concentração do NaOCl verificou-se um efeito mínimo, enquanto que a temperatura e o tempo de exposição teve uma relação significativa direta com a penetração de hipocloritos de sódio, especialmente aqueles com tensão superficial reduzido, nos túbulos dentinários. O tempo de exposição e temperatura do hipoclorito de sódio bem como a adição de agentes tensioativos pode influenciar significativamente a profundidade de penetração de soluções irrigantes nos túbulos dentinários.


Subject(s)
Humans , Dental Pulp Cavity/chemistry , Dentin/chemistry , Sodium Hypochlorite/chemistry , Surface-Active Agents/pharmacokinetics , Surface-Active Agents/chemistry
4.
Braz. j. pharm. sci ; 47(4): 769-778, Oct.-Dec. 2011. ilus, graf, tab
Article in English | LILACS | ID: lil-618070

ABSTRACT

The present investigation aims to evaluate an isotropic and thermodynamically stable nanoemulsion formulation for transdermal delivery of glycyrrhizin (GZ), with minimum surfactant and cosurfactant (Smix) concentrations that could improve its solubility, permeation enhancement, and stability. Pseudo-ternary phase diagrams were developed and various nanoemulsion formulations were prepared using soyabean oil as oil, Span 80, Brij 35 as a surfactant and isopropyl alcohol as a cosurfactant. Nanoemulsion formulations that passed the thermodynamic stability tests were characterized for pH, viscosity and droplet size using a transmission electron microscopy. The transdermal ability of glycyrrhizin through human cadaver skin was determined using Franz diffusion cells. The in vitro skin permeation profile of the optimized nanoemulsion formulation (NE2) was compared to that of conventional gel. A significant increase in permeability parameters such as steady-state flux (Jss) and permeability coefficient (Kp) was observed in the optimized nanoemulsion formulation (NE2), which consisted of 1 percent wt/wt of mono ammonium glycyrrhizinate (MAG), 32.4 percent Span 80, 3.7 percent Brij 35, 10 percent isopropyl alcohol, 46.5 percent soyabean oil and 6.4 percent distilled water. No obvious skin irritation was observed for the studied nanoemulsion formulation (NE2) or the gel. The results indicated that nanoemulsions are promising vehicles for transdermal delivery of glycyrrhizin through human cadaver skin, without the use of additional permeation enhancers, because excipients of nanoemulsions act as permeation enhancers themselves.


O objetivo da investigação é avaliar uma nanoemulsão isotrópica termodinamicamente estável para a administração transdérmica da glicirrizina (GZ), com concentrações mínimas de tensoativo e co-tensoativo (Smix), que poderiam melhorar a sua solubilidade, a permeação e a estabilidade. Os diagramas pseudo-ternários de fase foram desenvolvidos e diversas nanoemulsões foram preparadas com óleo de soja como óleo, Span 80, Brij 35 como tensoativos e álcool isopropílico como co-tensoativo. As nanoemulsões que passaram por testes de estabilidade termodinâmica foram caracterizadas por pH, viscosidade, tamanho de gota e microscopia eletrônica de transmissão. A capacidade transdérmica da glicirrizina em passar através da pele de cadáver humano foi determinada por células de difusão de Franz. O perfil in vitro de permeação cutânea da formulação otimizada (NE2) foi comparada com a de gel convencional. Observou-se aumento significativo nos parâmetros de permeabilidade, como fluxo de equilíbrio (JSS) e coeficiente de permeabilidade (Kp) na formulação otimizado (NE2), que consistiu de 1 por cento wt/wt de monoglicirrizinato de amônio (MAG), 32,4 por cento de Span 80, 3,7 por cento de Brij 35, 10 por cento de álcool isopropílico, 46,5 por cento de óleo de soja e 6,4 por cento de água destilada. Não se observou irritação óbvia da pele para as nanoemulsões estudadas (NE2) ou de gel. Os resultados indicaram que nanoemulsões são promissores veículos para a administração transdérmica de glicirrizina através da pele de cadáveres humanos, sem o uso adicional de promotor de permeação, porque excipientes de nanoemulsões atuam como promotores de permeação.


Subject(s)
Administration, Cutaneous , Glycyrrhizic Acid/pharmacokinetics , Anti-Inflammatory Agents/pharmacokinetics , Surface-Active Agents/pharmacokinetics , In Vitro Techniques , Enhancer Elements, Genetic , Nanotechnology
5.
Z Naturforsch C J Biosci ; 61(3-4): 203-12, 2006.
Article in English | MEDLINE | ID: mdl-16729578

ABSTRACT

We characterized a newly isolated bacterium, designated as IR1, with respect to its ability to degrade polycyclic aromatic hydrocarbons (PAHs) and to produce biosurfactants. Isolated IR1 was identified as Pseudomonas putida by analysis of 16S rRNA sequences (99.6% homology). It was capable of utilizing two-, three- and four-ring PAHs but not hexadecane and octadecane as a sole carbon and energy source. PCR and DNA hybridization studies showed that enzymes involved in PAH metabolism were related to the naphthalene dioxygenase pathway. Observation of both tensio-active and emulsifying activities indicated that biosurfactants were produced by IR1 during growth on both water miscible and immiscible substrates. The biosurfactants lowered the surface tension of medium from 54.9 dN cm(-1) to 35.4 dN cm(-1) and formed a stable and compact emulsion with an emulsifying activity of 74% with diesel oil, when grown on dextrose. These findings indicate that this isolate may be useful for bioremediation of sites contaminated with aromatic hydrocarbons.


Subject(s)
Polycyclic Aromatic Hydrocarbons/pharmacokinetics , Pseudomonas/metabolism , Surface-Active Agents/pharmacokinetics , Base Sequence , DNA Primers , Gene Amplification , Polymerase Chain Reaction , Pseudomonas/genetics , Pseudomonas/growth & development
6.
Antonie Van Leeuwenhoek ; 85(1): 1-8, 2004 Jan.
Article in English | MEDLINE | ID: mdl-15028876

ABSTRACT

Pseudomonas aeruginosa LBI isolated from petroleum-contaminated soil produced rhamnolipids (RL(LBI)) when cultivated on soapstock as the sole carbon source. HPLC-MS analysis of the purified culture supernatant identified 6 RL homologues (%): R(2) C(10) C(10) 28.9; R(2) C(10) C(12:1) 23.0; R(1) C(10) C(10) 23.4; R(2) C(10) C(12) 11.3; R(2) C(10) C(12) 7.9; R(2) C(10) C(12) 5.5. To assess the potential antimicrobial activity of the new rhamnolipid product, RL(LBI), its physicochemical properties were studied. RL(LBI) had a surface tension of 24 mN m(-1) and an interfacial tension of 1.31 mN m(-1); the cmc was 120 mg l(-1). RL(LBI) produced stable emulsions with hydrocarbons and vegetable oils. This product showed good antimicrobial behaviour against bacteria: MIC for Bacillus subtilis, Staphylococcus aureus and Proteus vulgaris was 8 mg l(-1), for Streptococcus faecalis 4 mg l(-1), and for Pseudomonas aeruginosa 32 mg l(-1). RL(LBI) was active against phytopathogenic fungal species, MIC values of 32 mg l(-1) being found against Penicillium, Alternaria, Gliocadium virens and Chaetonium globosum. Due to its physicochemical properties and antimicrobial behaviour, RL(LBI) could be used in bioremediation treatment and in the food, cosmetic and pharmaceutical industries.


Subject(s)
Pseudomonas aeruginosa/metabolism , Surface-Active Agents/metabolism , Surface-Active Agents/pharmacokinetics , Chromatography, High Pressure Liquid , Glycolipids/metabolism , Glycolipids/pharmacology , Kinetics , Microbial Sensitivity Tests , Petroleum , Pseudomonas aeruginosa/drug effects , Pseudomonas aeruginosa/growth & development , Pseudomonas aeruginosa/isolation & purification , Spectrometry, Mass, Electrospray Ionization , Surface-Active Agents/chemistry , Surface-Active Agents/isolation & purification
7.
Biopharm Drug Dispos ; 24(3): 95-103, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12673667

ABSTRACT

Albendazole (ABZ) is a widely used broad-spectrum benzimidazole (BZD) anthelmintic. Low hydrosolubility and poor/erratic gastrointestinal (GI) absorption play against the systemic availability and resultant clinical efficacy of BZD compounds. Different strategies are currently investigated to improve their bioavailability and efficacy in different animal species and humans. Surfactant agents facilitate dissolution of lipophilic drugs and increase membrane permeability. The influence of amphiphilic surfactants on the pattern of absorption and systemic availability of ABZ and its metabolites in cattle was characterized in the current trial. Twenty (20) parasite-free Holstein calves (100-120 kg) were randomly allocated into four groups and treated intraruminally (10 mg/kg) using one of the following ABZ suspensions: control without surfactant (75/25 dimetyl sulphoxide/saline solution) (group A), 5 mM sodium taurocholate (STC) in saline solution (group B), 8.27 mM sodium lauryl sulphate (SLS) in saline solution (group C) and a commercial formulation (Valbazen((R)), Pfizer Inc. SA) (group D). Jugular blood samples were taken over 72 h post-treatment and plasma analysed by HPLC. Albendazole sulphoxide (ABZSO) and sulphone were the metabolites found in plasma. STC did not affect ABZ absorption while increased ABZSO peak plasma concentration (C(max)) (158% higher, P<0.001) was observed following co-administration of ABZ plus SLS, compared to the control group without surfactant. ABZSO plasma availability was significantly greater after the ABZ-SLS (164%) co-administration compared to that obtained in the control group without surfactant. A similar ABZSO plasma availability was obtained following the treatments with the ABZ-SLS and the commercially available formulation. SLS-mediated enhanced dissolution and absorption of ABZ accounted for the observed increased systemic availability of the active ABZSO metabolite in cattle. These results should be considered among strategies to improve the use of BZD anthelmintics.


Subject(s)
Albendazole/pharmacokinetics , Intestinal Absorption/drug effects , Intestinal Absorption/physiology , Surface-Active Agents/pharmacokinetics , Albendazole/pharmacology , Animals , Cattle , Chemistry, Pharmaceutical , Surface-Active Agents/pharmacology
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