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1.
J Funct Biomater ; 14(5)2023 Apr 28.
Article in English | MEDLINE | ID: mdl-37233358

ABSTRACT

A significant amount of research has been conducted on applying functional materials as surgical sutures. Therefore, research on how to solve the shortcomings of surgical sutures through available materials has been given increasing attention. In this study, hydroxypropyl cellulose (HPC)/PVP/zinc acetate nanofibers were coated on absorbable collagen sutures using an electrostatic yarn winding technique. The metal disk of an electrostatic yarn spinning machine gathers nanofibers between two needles with positive and negative charges. By adjusting the positive and negative voltage, the liquid in the spinneret is stretched into fibers. The selected materials are toxicity free and have high biocompatibility. Test results indicate that the nanofiber membrane comprises evenly formed nanofibers despite the presence of zinc acetate. In addition, zinc acetate can effectively kill 99.9% of E. coli and S. aureus. Cell assay results indicate that HPC/PVP/Zn nanofiber membranes are not toxic; moreover, they improve cell adhesion, suggesting that the absorbable collagen surgical suture is profoundly wrapped in a nanofiber membrane that exerts antibacterial efficacy and reduces inflammation, thus providing a suitable environment for cell growth. The employment of electrostatic yarn wrapping technology is proven effective in providing surgical sutures with antibacterial efficacy and a more flexible range of functions.

2.
J Orthop Surg Res ; 17(1): 467, 2022 Oct 28.
Article in English | MEDLINE | ID: mdl-36307815

ABSTRACT

BACKGROUND: Studies have reported mixed results on the importance of medial calcar support for the treatment of proximal humeral fractures. The purpose of this study was to compare radiographic and functional outcomes of patients who had displaced proximal humeral fractures with varying levels of medial support. METHODS: We performed a retrospective comparative cohort study. The study was conducted at a Level III trauma center in Taiwan. Seventy patients with proximal humeral fractures were collected retrospectively from 2015 to 2019. Only patients with two-, three-, or four-part types (Neer type I, II, or III) of displaced proximal humeral fractures were included in this study. However, patients with head-split fracture patterns, shoulder dislocation, prior shoulder trauma, and poor fracture reduction present in postoperative films were excluded. We assessed the radiographic outcomes, including the reduction score and amount of impaction in the humeral head. The functional outcome was evaluated based on the Constant score. RESULTS: Patients were grouped into the intact medial calcar group and the medial calcar deficiency group. In a subgroup analysis, the group with intact medial support had a significantly lower amount of impaction and a higher Constant score compared with the medial calcar deficiency group. Additionally, the groups with intact medial support had a nonsignificant difference in the Constant score between the affected side and the contralateral side. CONCLUSION: The amount of impaction and the reduction score in the humeral head at the 12-month radiographic follow-up were significantly higher in the group with  medial support deficiency. However, the reduction score after surgery exhibited no difference. This implies that the inherent nature of medial comminution of proximal humeral fracture may lead to inferior radiographic outcomes.


Subject(s)
Humeral Fractures , Shoulder Fractures , Humans , Retrospective Studies , Bone Plates , Fracture Fixation, Internal/methods , Cohort Studies , Shoulder Fractures/diagnostic imaging , Shoulder Fractures/surgery , Treatment Outcome
3.
J Clin Med ; 11(18)2022 Sep 14.
Article in English | MEDLINE | ID: mdl-36143034

ABSTRACT

Background: Achilles tendon ruptures are one of the most common sports injuries. Recently, platelet-rich plasma (PRP) has been widely used in tendon-related disorders to enhance tendon healing. However, studies regarding PRP treatment in Achilles tendon rupture show inconsistent results. The purpose of this study was to evaluate the effectiveness of PRP in patients with acute Achilles tendon rupture treated with endoscopy-assisted percutaneous repair. Methods: A total of 62 patients with acute Achilles tendon rupture treated with surgical repair from January 2014 to December 2018 were enrolled in this study. Surgical repair in conjunction with PRP augmentation after surgery was classified as the PRP group. Surgical repair without PRP augmentation was classified as the non-PRP group. All patients were followed up at least 2 years post-operation. The outcomes were evaluated on the basis of rate of return to sports, time to return to play, Achilles Tendon Total Rupture Score (ATRS), calf circumference ratio, ankle range of motion (ROM) and complications following surgery. Results: At 2-year follow-up, the ATRS score was not significantly different between groups (p = 0.8), but the ATRS score in both groups improved with time. Rate of return to sports and time to return to play were not different between the two groups (p = 1.00). Moreover, calf circumference ratio and ankle ROM were evaluated at 6-month, 12-month, 18-month and 24-month follow-ups. At 6 months, the PRP group had better ankle ROM (p = 0.003) and a higher calf circumference ratio (p = 0.011); however, at the 24-month evaluation, there were no between-group differences regarding calf circumference ratio, ankle dorsiflexion and plantarflexion (p > 0.05). Conclusion: We show that PRP augmentation in Achilles tendon surgery did not yield superior functional and clinical outcomes. Therefore, clinicians should inform patients of the above information when undergoing Achilles tendon surgery and offer correct expectations to family and patients regrading PRP treatment.

4.
ACS Appl Bio Mater ; 5(2): 642-649, 2022 02 21.
Article in English | MEDLINE | ID: mdl-35080840

ABSTRACT

We report a potential biomedical material, NbTaTiVZr, and the impact of surface roughness on the osteoblast culture and later behavior based on in vitro tests of preosteoblasts. Cell activities such as adhesion, viability, and typical protein activity on NbTaTiVZr showed comparable results with that of commercially pure Ti (CP-Ti). In addition, NbTaTiVZr with a smooth surface exhibits better cell adhesion, viability, and typical protein activity which shows that surface modification can improve the biocompatibility of NbTaTiVZr. This supports the biological evidence and shows that NbTaTiVZr can potentially be evaluated as a biomedical material for clinical use.


Subject(s)
Osteoblasts , Titanium , Biocompatible Materials/metabolism , Cell Adhesion , Surface Properties , Titanium/pharmacology
5.
Biomed Res Int ; 2019: 4370382, 2019.
Article in English | MEDLINE | ID: mdl-31687390

ABSTRACT

BACKGROUND: Studies of previous cohorts have demonstrated a controversial association between extreme body mass index (BMI) and complication rates following total hip arthroplasty (THA). The purpose of this study was to compare 30-day perioperative complications in underweight (BMI <18.50 kg/m2), normal-weight (BMI 18.50-24.99 kg/m2), overweight (BMI 25.00-29.99 kg/m2), class I obesity (BMI 30.00-34.99 kg/m2), and morbidly obese (BMI ≥35.00 kg/m2) groups. METHODS: We performed a cohort study including patients who underwent unilateral primary THA by a single surgeon between January 2010 and December 2015 at our institution. We assessed 30-day complications, operation time, operative blood loss, and length of hospital stay. RESULTS: We identified 1565 primary THAs that were performed in patients with varying BMI levels. Compared with the normal-weight patients, the morbidly obese group had a higher 30-day complication rate (8.9% vs. 2.4%), longer operative time (79 minutes vs. 70 minutes), and more blood loss (376 mL vs. 302 mL). Underweight patients did not present any 30-day complications, and there were no differences among underweight and normal-weight patients regarding complication rates, operative time, or blood loss. The mean length of hospital stay was comparable among the different BMI groups. In the multivariate regression model, higher BMI was not associated with a higher risk of 30-day complications. Independent risk factors for 30-day complications were advanced age, prolonged operative time, and cardiovascular comorbidities. CONCLUSION: Although increased operative time, blood loss, and perioperative complications were seen in the morbidly obese patients, BMI alone was not an independent risk factor for a higher 30-day complication rate. Therefore, our data suggest clinicians should make elderly patients aware of increased 30-day complications before the procedure, particularly those with cardiovascular comorbidities. Withholding THA solely on the basis of BMI is not justified.


Subject(s)
Overweight/physiopathology , Postoperative Complications/etiology , Thinness/physiopathology , Adolescent , Adult , Aged , Aged, 80 and over , Arthroplasty, Replacement, Hip/methods , Arthroplasty, Replacement, Knee/methods , Body Mass Index , Cohort Studies , Comorbidity , Female , Humans , Length of Stay , Male , Middle Aged , Obesity, Morbid/complications , Obesity, Morbid/physiopathology , Operative Time , Prospective Studies , Retrospective Studies , Young Adult
6.
J Food Drug Anal ; 26(3): 1097-1104, 2018 07.
Article in English | MEDLINE | ID: mdl-29976402

ABSTRACT

To obtain the angiotension-I converting enzyme inhibitor (ACEI), a fusion ACEI polypeptide encoded with 8 DNA sequences of GPL, GPM, IKW, IVY, IRPVQ, IWHHT, IYPRY and IAPG, which were selected and designed and cloned into pGAPZαC and then transformed into Pichia pastoris SMD1168H. After 3 days induction, the fraction with highest ACEI activity was expressed and purified using a Ni Sepharose™ 6 Fast Flow. The IC50 of recombinant ACEI polypeptide was 88.2 µM. A 128-fold increase of ACEI activity (0.69 µM) was obtained after pepsin digestion, which was equivalent to 0.022 µM of captopril. Reverse phase HPLC indicated all the 8 peptides contained in ACEI-hydrolysate after pepsin digestion.


Subject(s)
Angiotensin-Converting Enzyme Inhibitors/metabolism , Gene Expression , Peptides/genetics , Pichia/genetics , Amino Acid Sequence , Angiotensin-Converting Enzyme Inhibitors/chemistry , Angiotensin-Converting Enzyme Inhibitors/isolation & purification , Cloning, Molecular , Genetic Vectors/genetics , Genetic Vectors/metabolism , Humans , Peptides/chemistry , Peptides/isolation & purification , Peptides/metabolism , Peptidyl-Dipeptidase A/chemistry , Pichia/metabolism , Transformation, Genetic
7.
Med Dosim ; 39(2): 139-45, 2014.
Article in English | MEDLINE | ID: mdl-24661778

ABSTRACT

With traditional photon therapy to treat large postoperative pancreatic target volume, it often leads to poor tolerance of the therapy delivered and may contribute to interrupted treatment course. This study was performed to evaluate the potential advantage of using passive-scattering (PS) and modulated-scanning (MS) proton therapy (PT) to reduce normal tissue exposure in postoperative pancreatic cancer treatment. A total of 11 patients with postoperative pancreatic cancer who had been previously treated with PS PT in University of Pennsylvania Roberts Proton Therapy Center from 2010 to 2013 were identified. The clinical target volume (CTV) includes the pancreatic tumor bed as well as the adjacent high-risk nodal areas. Internal (iCTV) was generated from 4-dimensional (4D) computed tomography (CT), taking into account target motion from breathing cycle. Three-field and 4-field 3D conformal radiation therapy (3DCRT), 5-field intensity-modulated radiation therapy, 2-arc volumetric-modulated radiation therapy, and 2-field PS and MS PT were created on the patients' average CT. All the plans delivered 50.4Gy to the planning target volume (PTV). Overall, 98% of PTV was covered by 95% of the prescription dose and 99% of iCTV received 98% prescription dose. The results show that all the proton plans offer significant lower doses to the left kidney (mean and V18Gy), stomach (mean and V20Gy), and cord (maximum dose) compared with all the photon plans, except 3-field 3DCRT in cord maximum dose. In addition, MS PT also provides lower doses to the right kidney (mean and V18Gy), liver (mean dose), total bowel (V20Gy and mean dose), and small bowel (V15Gy absolute volume ratio) compared with all the photon plans and PS PT. The dosimetric advantage of PT points to the possibility of treating tumor bed and comprehensive nodal areas while providing a more tolerable treatment course that could be used for dose escalation and combining with radiosensitizing chemotherapy.


Subject(s)
Pancreatic Neoplasms/radiotherapy , Proton Therapy/methods , Radiation Dosage , Radiotherapy Planning, Computer-Assisted , Radiotherapy, Intensity-Modulated/methods , Humans , Pancreatic Neoplasms/surgery , Retrospective Studies
8.
Virol J ; 8: 471, 2011 Oct 14.
Article in English | MEDLINE | ID: mdl-21999493

ABSTRACT

BACKGROUND: Japanese encephalitis virus (JEV) is a member of the mosquito-borne Flaviviridae family of viruses that causes human encephalitis. Upon infection of a new host, replication of viral RNA involves not only the viral RNA-dependent RNA polymerase (RdRp), but also host proteins. Host factors involved in JEV replication are not well characterized. RESULTS: We identified Hdj2, a heat-shock protein 40 (Hsp40)/DnaJ homolog, from a mouse brain cDNA library interacting with JEV nonstructural protein 5 (NS5) encoding viral RdRp using yeast two-hybrid system. Specific interaction of Hdj2 with NS5 was confirmed by coimmunoprecipitation and colocalization in JEV-infected cells. Overexpression of Hdj2 in JEV-infected cells led to an increase of RNA synthesis, and the virus titer was elevated approximately 4.5- to 10-fold. Knocking down of Hdj2 by siRNA reduced the virus production significantly. CONCLUSIONS: We conclude that Hdj2 directly associates with JEV NS5 and facilitates viral replication. This study is the first to demonstrate Hdj2 involved in JEV replication, providing insight into a potential therapeutic target and cell-based vaccine development of JEV infection.


Subject(s)
Encephalitis Virus, Japanese , Encephalitis, Japanese/virology , HSP40 Heat-Shock Proteins/metabolism , Host-Pathogen Interactions , Viral Nonstructural Proteins/metabolism , Virus Replication/genetics , Animals , Cell Line , Encephalitis Virus, Japanese/genetics , Encephalitis Virus, Japanese/metabolism , Gene Expression , Gene Library , Gene Silencing/drug effects , HSP40 Heat-Shock Proteins/chemistry , HSP40 Heat-Shock Proteins/genetics , Humans , Immunoprecipitation , Mice , Polymerase Chain Reaction , RNA, Small Interfering/pharmacology , RNA, Viral/biosynthesis , RNA-Dependent RNA Polymerase/genetics , RNA-Dependent RNA Polymerase/metabolism , Republic of Korea/epidemiology , Two-Hybrid System Techniques , Viral Nonstructural Proteins/chemistry , Viral Nonstructural Proteins/genetics
9.
J Gen Virol ; 92(Pt 12): 2803-2809, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21813703

ABSTRACT

Five host cellular proteins were identified in the secretion medium from Japanese encephalitis virus (JEV)-infected baby hamster kidney-21 (BHK-21) cells, including three molecular chaperones: Hsp70, GRP78 and Hsp90. Hsp90 isoforms were characterized further. Hsp90α was observed to be retained inside the nuclei, whereas Hsp90ß associated with virus particles during assembly and was released into the secretion medium upon JEV infection. The association of Hsp90ß and viral E protein was demonstrated by using sucrose-density fractionation and Western blot analysis. Moreover, JEV viral RNA replication was not affected by treatment with geldanamycin, an Hsp90 inhibitor, but impaired virus infectivity that was determined by a plaque-forming assay. Our results show that Hsp90ß, not Hsp90α, is present in the JEV-induced secretion medium and is required for JEV infectivity in BHK-21 cells.


Subject(s)
Encephalitis Virus, Japanese/genetics , HSP90 Heat-Shock Proteins/isolation & purification , HSP90 Heat-Shock Proteins/metabolism , Animals , Benzoquinones/pharmacology , Blotting, Western , Cell Line , Cricetinae , Encephalitis Virus, Japanese/pathogenicity , Encephalitis Virus, Japanese/physiology , HSP70 Heat-Shock Proteins/isolation & purification , HSP70 Heat-Shock Proteins/metabolism , HSP90 Heat-Shock Proteins/antagonists & inhibitors , Lactams, Macrocyclic/pharmacology , Protein Isoforms/isolation & purification , Protein Isoforms/metabolism , RNA, Viral/genetics , RNA, Viral/metabolism , Viral Proteins/genetics , Viral Proteins/metabolism , Virus Replication
10.
Virol J ; 8: 128, 2011 Mar 20.
Article in English | MEDLINE | ID: mdl-21418596

ABSTRACT

The serum-free medium from Japanese encephalitis virus (JEV) infected Baby Hamster Kidney-21 (BHK-21) cell cultures was analyzed by liquid chromatography tandem mass spectrometry (LC-MS) to identify host proteins that were secreted upon viral infection. Five proteins were identified, including the molecular chaperones Hsp90, GRP78, and Hsp70. The functional role of GRP78 in the JEV life cycle was then investigated. Co-migration of GRP78 with JEV particles in sucrose density gradients was observed and co-localization of viral E protein with GRP78 was detected by immunofluorescence analysis in vivo. Knockdown of GRP78 expression by siRNA did not effect viral RNA replication, but did impair mature viral production. Mature viruses that do not co-fractionate with GPR78 displayed a significant decrease in viral infectivity. Our results support the hypothesis that JEV co-opts host cell GPR78 for use in viral maturation and in subsequent cellular infections.


Subject(s)
Encephalitis Virus, Japanese/physiology , Encephalitis, Japanese/virology , Endoplasmic Reticulum/virology , Heat-Shock Proteins/metabolism , Animals , Cell Line , Cricetinae , Encephalitis Virus, Japanese/genetics , Encephalitis, Japanese/metabolism , Endoplasmic Reticulum/metabolism , Endoplasmic Reticulum Chaperone BiP , Heat-Shock Proteins/genetics , Host-Pathogen Interactions , Humans , Protein Transport , Virus Replication
11.
J Colloid Interface Sci ; 352(1): 186-93, 2010 Dec 01.
Article in English | MEDLINE | ID: mdl-20832810

ABSTRACT

The transition boundaries of various regimes characterizing the impact outcomes of a droplet upon a liquid layer of small thickness were investigated experimentally. With careful control of film thickness, the onset of these regimes in terms of a Weber number (We), which expresses the ratio between the droplet inertia and surface force, specifically when the layer depth is smaller than the droplet diameter, has been further clarified, as compared to prior studies. Several turning, non-monotonic trends between We and the film thickness normalized by the droplet diameter, H, were thus identified as H≲1. Furthermore, by adding various percentages of glycerine, the effects of liquid viscosity were revealed, which inhibited disintegration into secondary droplets. We also added surfactant to change the surface tension, leading to further complication of the collision outcome that would be related to the interaction between the crater and the bottom surface. The material effect of the solid surface was hence studied for further demonstration of such interplays. The results showed that increasing viscosity would essentially delay the occurrence of these transitions whereas reducing surface tension might encourage the onset. Therefore a possibility of using additives to manipulate the collision outcomes, while not changing much the constituent fluid properties, is presented.

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