弹性渗透胶囊模拟大丸注射,具有高缓释延迟破裂。

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Veronica Hidalgo-Alvarez , Kerr D.G. Samson , Vasiliki Kolyva , Yadunand Mani Koth , Cameron I. Cumming , Alex G. Leman , Lindsey A. Waddell , Vicki Stone , Jayne C. Hope , Ferry P.W. Melchels
{"title":"弹性渗透胶囊模拟大丸注射,具有高缓释延迟破裂。","authors":"Veronica Hidalgo-Alvarez ,&nbsp;Kerr D.G. Samson ,&nbsp;Vasiliki Kolyva ,&nbsp;Yadunand Mani Koth ,&nbsp;Cameron I. Cumming ,&nbsp;Alex G. Leman ,&nbsp;Lindsey A. Waddell ,&nbsp;Vicki Stone ,&nbsp;Jayne C. Hope ,&nbsp;Ferry P.W. Melchels","doi":"10.1016/j.ijpharm.2025.125550","DOIUrl":null,"url":null,"abstract":"<div><div>The need for repeated administration of vaccines is costly, logistically challenging and leads to reduced compliance. Osmosis-driven swelling and rupture has been proposed as a mechanism for delayed burst release to mimic follow-up (booster) injections without requiring further intervention. The use of microparticles does not guarantee a single bolus release, and previous studies using monolithic implants failed to demonstrate high instant release at the moment of burst. In this study we developed elastic capsules based on a caprolactone-lactide copolymer that released 75 ± 8 % of their contents instantly after up to several weeks of incubation. Capsules swelled up to 5x their original mass through highly reproducible osmosis-induced water uptake. The water uptake rates depended on osmotic strength and could be approximated with a numerical model revealing a water permeability of 3.6 ± 0.2 mm<sup>2</sup>/(Pa∙day) for all 118 capsules. The moment of burst depended on osmotic strength and capsule stiffness (median times varied from 16 to 37 days) and showed large scatter. The capsule material was non-toxic to a macrophage cell line and degraded through bulk hydrolysis, with an extrapolated completion time of 8 months. The capsules were administered successfully in bovine cadavers with a widely used applicator.</div></div>","PeriodicalId":14187,"journal":{"name":"International Journal of Pharmaceutics","volume":"676 ","pages":"Article 125550"},"PeriodicalIF":5.3000,"publicationDate":"2025-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Elastic osmotic capsules mimic bolus injection with high release at delayed burst\",\"authors\":\"Veronica Hidalgo-Alvarez ,&nbsp;Kerr D.G. Samson ,&nbsp;Vasiliki Kolyva ,&nbsp;Yadunand Mani Koth ,&nbsp;Cameron I. Cumming ,&nbsp;Alex G. Leman ,&nbsp;Lindsey A. Waddell ,&nbsp;Vicki Stone ,&nbsp;Jayne C. Hope ,&nbsp;Ferry P.W. Melchels\",\"doi\":\"10.1016/j.ijpharm.2025.125550\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The need for repeated administration of vaccines is costly, logistically challenging and leads to reduced compliance. Osmosis-driven swelling and rupture has been proposed as a mechanism for delayed burst release to mimic follow-up (booster) injections without requiring further intervention. The use of microparticles does not guarantee a single bolus release, and previous studies using monolithic implants failed to demonstrate high instant release at the moment of burst. In this study we developed elastic capsules based on a caprolactone-lactide copolymer that released 75 ± 8 % of their contents instantly after up to several weeks of incubation. Capsules swelled up to 5x their original mass through highly reproducible osmosis-induced water uptake. The water uptake rates depended on osmotic strength and could be approximated with a numerical model revealing a water permeability of 3.6 ± 0.2 mm<sup>2</sup>/(Pa∙day) for all 118 capsules. The moment of burst depended on osmotic strength and capsule stiffness (median times varied from 16 to 37 days) and showed large scatter. The capsule material was non-toxic to a macrophage cell line and degraded through bulk hydrolysis, with an extrapolated completion time of 8 months. The capsules were administered successfully in bovine cadavers with a widely used applicator.</div></div>\",\"PeriodicalId\":14187,\"journal\":{\"name\":\"International Journal of Pharmaceutics\",\"volume\":\"676 \",\"pages\":\"Article 125550\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2025-04-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Pharmaceutics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0378517325003874\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Pharmaceutics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378517325003874","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

需要重复接种疫苗费用高昂,在后勤上具有挑战性,并导致依从性降低。渗透驱动的肿胀和破裂被认为是延迟破裂释放的机制,以模拟后续(加强)注射,而无需进一步干预。微颗粒的使用并不能保证单丸释放,先前使用单片植入物的研究未能证明在破裂时具有高的瞬间释放。在这项研究中,我们开发了基于自内酯-丙交酯共聚物的弹性胶囊,在长达几周的孵育后,其含量立即释放75 ± 8 %。通过高度可复制的渗透诱导的水分吸收,胶囊膨胀到原来质量的5倍。水分吸收速率取决于渗透强度,可以用一个数值模型来近似表示,所有118个胶囊的渗透率为3.6 ± 0.2 mm2/(Pa∙day)。破裂时刻取决于渗透强度和包膜刚度(中位时间为16 ~ 37 d),并表现出较大的离散性。胶囊材料对巨噬细胞系无毒,通过大量水解降解,外推完成时间为8 个月。用广泛使用的涂抹器成功地在牛尸体中施用了胶囊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Elastic osmotic capsules mimic bolus injection with high release at delayed burst

Elastic osmotic capsules mimic bolus injection with high release at delayed burst
The need for repeated administration of vaccines is costly, logistically challenging and leads to reduced compliance. Osmosis-driven swelling and rupture has been proposed as a mechanism for delayed burst release to mimic follow-up (booster) injections without requiring further intervention. The use of microparticles does not guarantee a single bolus release, and previous studies using monolithic implants failed to demonstrate high instant release at the moment of burst. In this study we developed elastic capsules based on a caprolactone-lactide copolymer that released 75 ± 8 % of their contents instantly after up to several weeks of incubation. Capsules swelled up to 5x their original mass through highly reproducible osmosis-induced water uptake. The water uptake rates depended on osmotic strength and could be approximated with a numerical model revealing a water permeability of 3.6 ± 0.2 mm2/(Pa∙day) for all 118 capsules. The moment of burst depended on osmotic strength and capsule stiffness (median times varied from 16 to 37 days) and showed large scatter. The capsule material was non-toxic to a macrophage cell line and degraded through bulk hydrolysis, with an extrapolated completion time of 8 months. The capsules were administered successfully in bovine cadavers with a widely used applicator.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
10.70
自引率
8.60%
发文量
951
审稿时长
72 days
期刊介绍: The International Journal of Pharmaceutics is the third most cited journal in the "Pharmacy & Pharmacology" category out of 366 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信