Backflow reduction in local injection therapy with gelatin formulations.

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Drug Delivery Pub Date : 2024-12-01 Epub Date: 2024-03-22 DOI:10.1080/10717544.2024.2329100
Kazuki Kotani, Francois Marie Ngako Kadji, Yoshinobu Mandai, Yosuke Hiraoka
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引用次数: 0

Abstract

The local injection of therapeutic drugs, including cells, oncolytic viruses and nucleic acids, into different organs is an administrative route used to achieve high drug exposure at the site of action. However, after local injection, material backflow and side effect reactions can occur. Hence, this study was carried out to investigate the effect of gelatin on backflow reduction in local injection. Gelatin particles (GPs) and hydrolyzed gelatin (HG) were injected into tissue models, including versatile training tissue (VTT), versatile training tissue tumor-in type (VTT-T), and broiler chicken muscles (BCM), using needle gauges between 23 G and 33 G. The backflow material fluid was collected with filter paper, and the backflow fluid rate was determined. The backflow rate was significantly reduced with 35 μm GPs (p value < .0001) at different concentrations up to 5% and with 75 μm GPs (p value < .01) up to 2% in the tissue models. The reduction in backflow with HG of different molecular weights showed that lower-molecular-weight HG required a higher-concentration dose (5% to 30%) and that higher-molecular-weight HG required a lower-concentration dose (7% to 8%). The backflow rate was significantly reduced with the gelatin-based formulation, in regard to the injection volumes, which varied from 10 μL to 100 μL with VTT or VTT-T and from 10 μL to 200 μL with BCM. The 35 μm GPs were injectable with needles of small gauges, which included 33 G, and the 75 μm GPs and HG were injectable with 27 G needles. The backflow rate was dependent on an optimal viscosity of the gelatin solutions. An optimal concentration of GPs or HG can prevent material backflow in local injection, and further studies with active drugs are necessary to investigate the applicability in tumor and organ injections.

使用明胶制剂进行局部注射治疗时减少回流。
将治疗药物(包括细胞、溶瘤病毒和核酸)局部注射到不同器官,是在作用部位实现高药物暴露的一种管理途径。然而,局部注射后可能会出现物质回流和副作用反应。因此,本研究旨在探讨明胶对减少局部注射回流的影响。使用 23 G 至 33 G 的针规将明胶颗粒(GPs)和水解明胶(HGs)注射到组织模型中,包括多功能训练组织(VTT)、多功能训练组织肿瘤型(VTT-T)和肉鸡肌肉(BCM)。在组织模型中,不同浓度的 35 μm GPs(p 值 < .0001)和 75 μm GPs(p 值 < .01)的回流率分别明显降低到 5%和 2%(p 值 < .01)。不同分子量的 HG 可降低回流率,这表明低分子量的 HG 需要较高浓度的剂量(5% 至 30%),而高分子量的 HG 需要较低浓度的剂量(7% 至 8%)。明胶制剂的回流率明显降低,注射剂量方面,VTT 或 VTT-T 的回流率从 10 μL 到 100 μL 不等,BCM 的回流率从 10 μL 到 200 μL 不等。35 μm GPs 可使用小号针头(包括 33 G)注射,75 μm GPs 和 HG 可使用 27 G 针头注射。回流速度取决于明胶溶液的最佳粘度。最佳浓度的 GPs 或 HG 可以防止局部注射中的材料回流,有必要对活性药物进行进一步研究,以探讨其在肿瘤和器官注射中的适用性。
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
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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