托那伯沙眼给药转移体的制备与表征。

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Santosh Bhujbal, Ilva D Rupenthal, Priyanka Agarwal
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引用次数: 0

摘要

转移体(TFS)是一种可变形的囊泡,以其增强透皮药物渗透的能力而闻名。本研究旨在开发和优化TFS,以评估它们是否也能增强托纳伯沙(一种难溶性炎性体抑制剂)的眼部递送。采用Phospholipon®90G和Tween®80作为边缘活化剂制备TFS。使用全因子实验设计评估配方参数(边缘活化剂和冷冻保护剂浓度)对TFS特性的影响。进一步对优化后的TFS滴眼液进行粒径、zeta电位、可变形性、包封效率(EE)、药物含量、pH和渗透压的表征。此外,在不同的储存条件下,评价了TFS在3个月内的稳定性。最后,以含中链甘油三酯的托那伯沙溶液为对照,体外研究药物在眼部局部应用后对角膜、结膜、眼睑和巩膜-脉络膜的渗透。优化后的TFS形成球形单层囊泡,平均直径小于130 nm, EE大于80%,在-20°C和5±3°C条件下稳定达3个月。TFS滴眼液在不影响被测组织屏障特性的情况下,显著提高了眼部穿透性。比较药物在不同眼组织间的渗透情况,揭示TFS入眼的渗透机制。总的来说,这项研究表明TFS为托纳伯沙眼内输送提供了一个有希望的替代方案。
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 transfersomes for ocular delivery of tonabersat.

Transfersomes (TFS) are deformable vesicles, known for their ability to enhance transdermal drug penetration. This study aimed to evaluate whether TFS can also enhance ocular delivery of poorly soluble tonabersat. TFS were prepared using Phospholipon® 90G with Tween® 80 as the edge activator. The effect of formulation parameters (edge activator and cryoprotectant concentrations) on TFS characteristics were evaluated using a full factorial design. The optimized TFS eyedrop was characterized for particle size, zeta potential, deformability, entrapment efficiency (EE), drug content, pH, osmolality and TFS stability over 3 months at different storage conditions. Furthermore, drug penetration into the cornea, conjunctiva, eyelid, and sclera-choroid after topical application was studied ex vivo using a tonabersat solution in medium chain triglycerides as the control. The optimized TFS formed spherical unilamellar vesicles with a mean diameter <130 nm, EE >80%, and were stable at -20 and 5 ± 3 °C for up to 3 months. The TFS eyedrop resulted in significantly greater ocular penetration than the control without affecting the barrier properties of the tested tissues. Drug penetration into different ocular tissues was compared, shedding light on the penetration mechanism of TFS. Overall, this study demonstrates that TFS provide a promising alternative for the ocular delivery of tonabersat.

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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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