含有依非韦伦、恩曲他滨和替诺福韦的固定剂量微乳的配方和特性。

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Samantha Mabvira, Sandile M Khamanga, Roderick B Walker
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引用次数: 0

摘要

尽管与艾滋病毒/艾滋病有关的死亡率显著下降,但艾滋病毒仍然是特定人群的主要死亡原因之一。尽管人们共同努力寻找治愈艾滋病的方法,但迄今为止,还没有找到。目前的抗逆转录病毒疗法抑制了病毒的复制,但没有完全根除它。成功抑制病毒复制只能使用抗逆转录病毒药物组合来实现,这些药物在艾滋病毒生命周期的不同阶段抑制病毒复制。依非韦伦(EFV)、恩曲他滨(FTC)和富马酸替诺福韦二吡酯(TDF)是一种用于艾滋病毒管理的组合。研制了一种由EFV、FTC和TDF组成的新型固定剂量微乳配方。采用相滴定法制备微乳(ME),测定其载药量、粒径、透明度、Zeta电位和pH值。用透射电镜观察微乳。采用体外释放试验评价药物活性成分的释放行为。经动态光散射测定和透射电镜证实,优化后的ME平均Zeta电位为33.8 mV,液滴尺寸为117 nm。粉末x射线衍射和差示扫描量热分析揭示了药物分子分散的存在。这些发现表明,将ME作为一种固定剂量组合技术,用于输送EFV、FTC和TDF的潜在价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation and Characterization of a Fixed-Dose Microemulsion Containing Efavirenz, Emtricitabine, and Tenofovir.

Despite a marked decrease in HIV/AIDS-related mortality, HIV remains one of the leading causes of death in specific populations. Despite concerted efforts to find a cure for HIV, to date, none exists. Current antiretroviral therapy inhibits replication of the virus without completely eradicating it. The successful inhibition of viral replication is only achieved using a combination of antiretrovirals, which inhibit viral replication at different stages of the HIV lifecycle. Efavirenz (EFV), emtricitabine (FTC), and tenofovir disoproxil fumarate (TDF) are one combination used for HIV management. The development of a novel fixed-dose microemulsion formulation of EFV, FTC and TDF was undertaken. Microemulsions (ME) were manufactured using phase titration and drug loading, particle size, transparency, Zeta potential and pH were determined. Transmission Electron Microscopy was used to visualize the microemulsion. In-vitro release testing was used to evaluate active pharmaceutical ingredient release behaviour. The optimized ME had an average Zeta potential of 33.8 mV and droplet size of 117 nm, determined using Dynamic Light Scattering and confirmed using Transmission Electron Microscopy. Powder X-ray diffraction and Differential Scanning Calorimetry analysis revealed the presence of a molecular dispersion of drugs. These findings demonstrate the potential value of using ME as a fixed-dose combination technology for the delivery of EFV, FTC and TDF.

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来源期刊
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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