局部应用载伊卡唑纳米粒子的设计、开发与表征

Q3 Pharmacology, Toxicology and Pharmaceutics International Journal of Pharmaceutical Quality Assurance Pub Date : 2023-06-25 DOI:10.25258/ijpqa.14.2.20
S. Ahmad, K. Patil, Ganaraj Koli, B. A. Rahman, Lokesh Barde, Mahesh Deshpande, H. Tare
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引用次数: 0

摘要

背景和目的:硝酸益康唑(ECN)负载的纳米颗粒局部给药是当前研究的重点,旨在提高药物治疗真菌感染的局部疗效,同时减轻药物的胃肠道副作用。进一步的胶体载体方法被用作精确局部给药的方法。方法:乳化-扩散(E-D)法是制备纳米凝胶的一种替代方法,可以避免与乳化-蒸发技术相关的毒性溶剂问题。它的易用性、增强的稳定性和适应性都得到了各种研究小组的验证。ECN在稳定剂溶液中负载二氯甲烷,通过在高压下高速均化配制。添加具有重复均化循环的水相导致药物扩散到纳米凝胶中。进一步添加甘露醇作为冷冻保护剂和Carbabol 940作为胶凝剂使制剂稳定。结果:使用马尔文zetasizer测量了颗粒的典型尺寸、多分散指数(PDI)和ζ电位。在五种NFs中,冻干批次的NF3表现出最低的ζ电位(-11.6 mV)和PDI(0.208),表明组合物是稳定的。DSC和XRD分析揭示了ECN的非晶态转变。扫描电子显微照片显示了离散的圆形颗粒。评价了所选NLCs的凝胶分散体的存在、粘度和铺展能力。总的od77%的药物是从选定的ECN负载的纳米凝胶制剂中体外释放的。因此,可以合理地假设ECN负载的纳米凝胶是治疗真菌感染的有效药物递送系统,因为它们延长了药物释放的持续时间。结论:在退化条件下,不存在任何相互冲突的峰值。因此,开发了一种技术,由于其灵敏度、强度、准确性和稳定性,该技术具有高度适用性。
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Design, Development and Characterization of Econazole loaded Nanoparticles for Topical Application
Background and Objectives: Econazole nitrate (ECN) loaded nanoparticles with topical administration were the focus of the current study, which aimed to improve the topical efficacy of the medicine in treating fungal infections while also mitigating the drug’s gastrointestinal (GI) side effects. Further colloidal carrier methodology was employed as a method for the topical administration of medications with precision. Method: The emulsification-diffusion (E-D) method is an alternate approach for preparing nanogels that avoids the toxicitysolvent issues associated with the emulsification-evaporation technique. Its ease of use, enhanced stability, and adaptability have all been verified by a variety of research groups. ECN loaded with dichloromethane in stabilizer solution, formulated by high-speed homogenization at elevated pressure. The addition of aqueous phase with repeated homogenization cycles causes drug diffusion into nanogels. Further addition of mannitol as cryoprotectant and Carbapol 940 as gelling agent stabiles the formulation. Results: The typical size of the particles, polydispersity index (PDI), and zeta potential were all measured with the use of the Malvern zetasizer. Of the five NFs, the lyophilized batch of NF3 exhibited the lowest zeta potential (-11.6 mV) and the PDI (0.208), indicating that the composition was stable. DSC and XRD analysis revealed an amorphous transformation of ECN. The scanning electron micrograph demonstrated discrete, roundish particles. The existence, viscosity, and spreading ability of a gelled dispersion of the selected NLCs were evaluated. Total od 77% of the medication was released in-vitro from a chosen formulation of ECN-loaded nanogels. As a result, it is reasonable to assume that ECN-loaded nanogels are an effective drug delivery system for treating fungal infections since they prolong the duration of drug release. Conclusion: Under degraded conditions, there are not any peaks that conflict with one another. As a result, a technique was developed that is highly applicable due to its sensitivity, strength, accuracy, and demonstration of stability.
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来源期刊
International Journal of Pharmaceutical Quality Assurance
International Journal of Pharmaceutical Quality Assurance Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
0.80
自引率
0.00%
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0
期刊介绍: INTERNATIONAL JOURNAL OF PHARMACEUTICAL QUALITY ASSURANCE is a quarterly international journal publishing the finest peer-reviewed research in the field of Pharmaceutical Quality Assurance and Pharmaceutical Analysis on the basis of its originality, importance, disciplinary interest, timeliness, accessibility, elegance, and surprising conclusions. IJPQA also provides rapid, authoritative, insightful and arresting news and interpretation of topical and coming trends affecting science, scientists and the wider public.
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