Effect of surfactants and polymer composition on the characteristics of polyhydroxyalkanoate nanoparticles.

IF 4.3 Q2 CHEMISTRY, MEDICINAL
ADMET and DMPK Pub Date : 2025-06-04 eCollection Date: 2025-01-01 DOI:10.5599/admet.2723
Aleksei Dorokhin, Sergei Lipaikin, Galina Ryltseva, Alexander Shabanov, Kristina Sapozhnikova, Tatiana Volova, Sergei Kachin, Ekaterina Shishatskaya
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引用次数: 0

Abstract

Background and purpose: Polyhydroxyalkanoates (PHAs) are biodegradable polyesters of bacterial origin that are actively studied as matrices for the preparation of nanoparticulate drug delivery systems. The most significant parameters affecting PHAs nanoparticles (NPs) characteristics are polymer composition and the type of surfactant used to stabilize the emulsion during NPs preparation. However, there are only a few studies in the literature investigating the effect of these factors on the characteristics of PHA NPs.

Experimental approach: Blank poly(3-hydroxybutyrate) (P3HB) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (P3HBV) NPs were produced and characterized in terms of their size, morphology and zeta potential. Poly(vinyl alcohol) (PVA) with various molecular weights (31-50 and 85-124 kDa), as well as Tween 20 (TW20), Tween 80 (TW80), sodium deoxycholate (SDC) and sodium dodecyl sulphate (SDS) were used as surfactants. For NPs that formed stable aqueous suspensions and had the most desirable characteristics (P3HB/PVA31-50 and P3HBV/PVA31-50), hemolytic activity and cytotoxicity to HeLa and C2C12 cells in vitro were determined.

Key results: NPs of both P3HB and P3HBV obtained using PVA with the M w of 31-50 kDa as a surfactant had regular spherical shape, uniform size distribution, average diameter of about 900 nm and zeta potential of -28.5 and -28.7 mV, respectively. PVA85-124, TW20 and TW80, as well as SDC and SDS as surfactants, did not show satisfactory results due to suspension gelation, formation of hollow NPs with irregular shape and poor resuspension after washing and freeze-drying, respectively. P3HB/PVA31-50 and P3HBV/PVA31-50 NPs did not have hemolytic activity and did not show pronounced cytotoxicity to HeLa and C2C12 cells in the concentration range from 10 to 500 μg mL-1, so these samples were regarded as safe and biocompatible.

Conclusion: In this study, the effect of various non-ionic and anionic surfactants on the characteristics of P3HB and P3HBV NPs was investigated. PVA31-50 was found to be effective in producing NPs of both studied polymers with good biocompatibility and favorable characteristics, making them suitable for drug delivery applications. In contrast, other studied surfactants, i.e., PVA85-124, TW20, TW80, SDC and SDS, require further investigation. The obtained findings may promote the development of novel PHA-based nanomedicines.

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表面活性剂和聚合物组成对聚羟基烷酸酯纳米颗粒性能的影响。
背景和目的:聚羟基烷酸酯(PHAs)是细菌来源的可生物降解聚酯,被积极研究作为制备纳米颗粒药物递送系统的基质。影响聚相芳烃纳米颗粒(NPs)性能的最重要参数是聚合物组成和制备过程中用于稳定乳液的表面活性剂类型。然而,文献中只有少数研究探讨了这些因素对PHA NPs特性的影响。实验方法:制备空白聚(3-羟基丁酸酯)(P3HB)和聚(3-羟基丁酸酯-co-3-羟基戊酸酯)(P3HBV) NPs,并对其大小、形态和zeta电位进行表征。采用不同分子量(31-50和85-124 kDa)的聚乙烯醇(PVA)、Tween 20 (TW20)、Tween 80 (TW80)、脱氧胆酸钠(SDC)和十二烷基硫酸钠(SDS)作为表面活性剂。对于形成稳定的水悬浮液并具有最理想特性的NPs (P3HB/PVA31-50和P3HBV/PVA31-50),测定其体外对HeLa和C2C12细胞的溶血活性和细胞毒性。关键结果:以mw为31-50 kDa的PVA为表面活性剂得到的P3HB和P3HBV的NPs均呈规则的球形,粒径分布均匀,平均直径约为900 nm, zeta电位分别为-28.5和-28.7 mV。PVA85-124、TW20和TW80以及SDC和SDS作为表面活性剂,分别存在悬浮凝胶化、形成形状不规则的空心NPs、洗涤和冷冻干燥后重悬效果不理想的问题。在10 ~ 500 μg mL-1浓度范围内,P3HB/PVA31-50和P3HBV/PVA31-50 NPs对HeLa和C2C12细胞不具有溶血活性,细胞毒性不明显,因此认为这些样品是安全的,具有生物相容性。结论:本研究考察了各种非离子和阴离子表面活性剂对P3HB和P3HBV NPs特性的影响。PVA31-50被发现能有效地产生两种聚合物的NPs,具有良好的生物相容性和良好的特性,使其适合于药物传递应用。相比之下,其他已研究的表面活性剂,如PVA85-124、TW20、TW80、SDC和SDS,需要进一步研究。这些发现可能促进新型pha基纳米药物的开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ADMET and DMPK
ADMET and DMPK Multiple-
CiteScore
4.40
自引率
0.00%
发文量
22
审稿时长
4 weeks
期刊介绍: ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study
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