Practical approach to development of GS-445124-loaded PLGA nanoparticles for the long-term treatment of feline infectious peritonitis caused by feline coronavirus infection

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics Pub Date : 2025-04-15 Epub Date: 2025-03-17 DOI:10.1016/j.ijpharm.2025.125468
Minki Jin , Hyun-Jin Cho , Young-Guk Na , Taek-Seon Yun , Bomin Song , Sang-Rae Lee , Seonho Je , Hong-Geun Oh , Yang-Gyu Park , Jinhyung Rho , Mi‑Jin Yang , Jin Soo Shin , Jong-Suep Baek , Hong-Ki Lee , Tae-Won Kim , Cheong-Weon Cho
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Abstract

Feline infectious peritonitis virus (FIPV) caused by feline coronavirus (FCoV) infection leads to a high mortality rate when untreated. GS-441524, an antiviral agent effective against FIPV, is orally administered twice daily or through daily subcutaneous injections for approximately 12 weeks. While the short treatment period recuses concerns about adherence, frequent administrations may cause handling-related stress in cats. Therefore, it is essential to develop a long-acting formulation that requires only a single administration. In this study, we used polylactide-co-glycolide (PLGA) as a carrier, which was used to effectively encapsulate GS-441524 with sustained-release functionality and GS-441524-loaded PLGA nanoparticles (GS-PLGA NP) were prepared. The particle size of GS-PLGA NP was 216 nm, the encapsulation efficiency was 78 %, and the 7-day release was 92 %. When GS-PLGA NP was injected at 22 mg/kg in cats, higher systemic exposure can be expected compared to injecting GS-441524 at 4 mg/kg for one week (relative bioavailability, 152 %). As well as GS-PLGA NP showed lower toxicity, improved cellular uptake, and enhanced antiviral efficacy against FCoV compared to the pure GS-441524.

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负载gs -445124的PLGA纳米颗粒长期治疗猫冠状病毒感染引起的猫感染性腹膜炎的实用方法
由猫冠状病毒(FCoV)感染引起的猫传染性腹膜炎病毒(FIPV)在未经治疗的情况下死亡率很高。GS-441524是一种对FIPV有效的抗病毒药物,每日口服两次或每日皮下注射,持续约12 周。虽然治疗时间短可以避免对依从性的担忧,但频繁的给药可能会导致猫的处理相关压力。因此,开发一种只需单次给药的长效制剂至关重要。本研究以聚丙交酯-共聚物(PLGA)为载体,对具有缓释功能的GS-441524进行有效包封,制备了负载GS-441524的PLGA纳米颗粒(GS-PLGA NP)。GS-PLGA NP的粒径为216 nm,包封率为78 %,7 d释放度为92 %。当以22 mg/kg的剂量注射GS-PLGA NP时,与以4 mg/kg的剂量注射GS-441524一周相比,预计会有更高的全身暴露(相对生物利用度,152 %)。与纯化的GS-441524相比,GS-PLGA NP具有更低的毒性,改善细胞摄取,增强对FCoV的抗病毒功效。
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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.
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