D-peptide hydrogels as a long-acting multipurpose drug delivery platform for combined contraception and HIV prevention

药品 药理学 药物输送 化学 体内 蛋白酵素 自组装肽 自愈水凝胶 杀菌剂 医学 生物化学 人类免疫缺陷病毒(HIV) 免疫学 生物 生物技术 有机化学
作者
Sreekanth Pentlavalli,Sophie Coulter,Yuming An,Emily R. Cross,Han Sun,Jessica Moore,Akmal Bin Sabri,Brett Greer,Lalitkumar K. Vora,Helen O. McCarthy,Garry Laverty
出处
期刊:Journal of Controlled Release [Elsevier BV]
卷期号:379: 30-44 被引量:5
标识
DOI:10.1016/j.jconrel.2024.12.052
摘要

New multipurpose prevention technology products for use by women, focused on reducing HIV infection and preventing unwanted pregnancies, are a global health priority. Discreet long-acting formulations will empower women with greater choice around their sexual health. This paper outlines the development of a long-acting technology that enables multiple drugs to be incorporated within one injectable platform. This fixed-dose combination product is formed from a phosphorylated D-peptide (naphthalene-2-ly)-acetyl-diphenylalanine-lysine-tyrosine-glycine-OH (Napffky(p)G-OH) that enables the highly hydrophobic drugs MIV-150 (HIV antiretroviral) and etonogestrel (contraceptive) to be solubilized together within aqueous solvents. Upon subcutaneous injection, this D-peptide-drug combination self-assembles in response to phosphatase enzymes present within the skin space to form an in situ forming drug-releasing hydrogel depot. Oscillatory rheology confirmed the formation of hydrogels, which began within ~10 s exposure to 3.98 U/mL phosphatase enzymes and continued for ~198 mins for a Napffk(MIV-150)y(p)G-OH + Napffk(ENG)y(p)G-OH combination (8:2 ratio). Biostability against proteases, an important consideration for long-acting injectables, was demonstrated for at least 28 days in vitro. Covalent attachment of each drug to the D-peptide via an ester linkage enabled sustained release of the drug in an unmodified form via hydrolysis of the D-peptide-drug linker. This significantly reduced the initial drug burst. Low toxicity was also demonstrated in vitro via cell culture (MTS, LHS, Live/Dead®) and within in vivo studies (H&E staining). The fixed dose combination was able to deliver clinically relevant concentrations of each drug to Sprague-Dawley rats for 49 days, providing proof-of-concept for the use of hydrogel-forming D-peptides (Napffky(p)G-OH) as a long-acting injectable platform for the delivery of multiple hydrophobic drugs.
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