过氧化苯甲酰微海绵基痤疮感染透皮凝胶的研制及评价。

Q2 Pharmacology, Toxicology and Pharmaceutics
Samali S Raut, Neha R Singh, Bhushan R Rane, Ashish S Jain
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引用次数: 0

摘要

背景:过氧化苯甲酰是一种具有抗菌、刺激、溶角、溶粉刺和抗炎特性的过氧化物。当过氧化苯甲酰局部使用时,它会分解并释放氧气,杀死痤疮丙酸杆菌。过氧化苯甲酰的刺激性影响会导致上皮细胞更新增加,从而导致皮肤脱落,有助于粉刺的愈合。寻常痤疮的治疗包括使用过氧化苯甲酰。目的:研究以卡波波尔934为胶凝剂制备过氧化苯甲酰的微海绵凝胶制剂的配方,并对微海绵凝胶制剂的理化性能进行评价。方法:采用准乳法制备抗痤疮剂过氧化苯甲酰药物微海绵,并采用简单扩散池采用合适的膜模型体外释放。结果:干燥前,用蒸馏水过滤和冲洗微海绵。以过氧化苯甲酰与苦楝草RS100为原料,以1:4的比例组成的制剂,药物含量高达87.5%,得率高达78.20%。微海绵凝胶的药物含量为84%。采用柱杯法对金黄色葡萄球菌进行了微生物学研究,取得了较好的效果。微海绵制剂体外扩散持续8小时。根据聚合物:药物比(4:1),Eudragit RS-100在8 h后的释药率为88.87%。结论:采用准乳状溶剂扩散法,可以成功地制备出以淫羊藿RS100、乙基纤维素和HPMC K4M为聚合物的过氧化苯甲酰微海绵。以多孔聚合物Eudragit RS100为原料制备出给药浓度最高的配方。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation Of Benzoyl Peroxide Microsponge-Based Transdermal Gel For Acne Infection And Its Evaluation.

Background: Benzoyl peroxide is a peroxide with antibacterial, irritating, keratolytic, comedolytic, and anti-inflammatory properties. When benzoyl peroxide is applied topically, it breaks down and releases oxygen, which kills the germs of Propionibacterium acnes. Benzoyl peroxide's irritating impact causes an increase in epithelial cell turnover, which causes the skin to peel and aids in the healing of comedones. Treatment for acne vulgaris involves the use of benzoyl peroxide.

Objective: The research is aimed at studying the formulation of Microsponge gel preparation of benzoyl peroxide by using Carbopol 934 as a gelling agent and evaluation of microsponge gel formulation for its physicochemical properties.

Methods: Microsponges of Anti-acne agent benzoyl peroxide drug were prepared by quasi-emulsion method, and in-vitro drug release using a suitable membrane model using a simple diffusion cell.

Result: Prior to drying, the microsponge was filtered and rinsed using distilled water. Formulation containing benzoyl peroxide and Eudragit RS100 with a ratio of 1:4 showed a high 87.5% drug content and 78.20 % yield. The drug content of the microsponge gel was found to be 84%. Microbiological study on S. aureus was conducted by the cylinder cup method and found good results. The in-vitro diffusion of microsponge formulations was sustained for 8 hours. The drug release rate for Eudragit RS-100 was reported to be 88.87% after 8 hours based on the polymer: drug ratio (4:1).

Conclusion: The quasi-emulsion solvent diffusion method was used to successfully prepare benzoyl peroxide microsponges using Eudragit RS100, Ethyl Cellulose, and HPMC K4M as polymers. The formulations with the highest medication concentration were made with the porous polymer Eudragit RS100.

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来源期刊
Pharmaceutical nanotechnology
Pharmaceutical nanotechnology Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.20
自引率
0.00%
发文量
46
期刊介绍: Pharmaceutical Nanotechnology publishes original manuscripts, full-length/mini reviews, thematic issues, rapid technical notes and commentaries that provide insights into the synthesis, characterisation and pharmaceutical (or diagnostic) application of materials at the nanoscale. The nanoscale is defined as a size range of below 1 µm. Scientific findings related to micro and macro systems with functionality residing within features defined at the nanoscale are also within the scope of the journal. Manuscripts detailing the synthesis, exhaustive characterisation, biological evaluation, clinical testing and/ or toxicological assessment of nanomaterials are of particular interest to the journal’s readership. Articles should be self contained, centred around a well founded hypothesis and should aim to showcase the pharmaceutical/ diagnostic implications of the nanotechnology approach. Manuscripts should aim, wherever possible, to demonstrate the in vivo impact of any nanotechnological intervention. As reducing a material to the nanoscale is capable of fundamentally altering the material’s properties, the journal’s readership is particularly interested in new characterisation techniques and the advanced properties that originate from this size reduction. Both bottom up and top down approaches to the realisation of nanomaterials lie within the scope of the journal.
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