Determination of the Toxicity Preferences of Ocular Drug Delivery System by Comparing Two Different Toxicity Bioassays.

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS Assay and drug development technologies Pub Date : 2023-10-01 DOI:10.1089/adt.2023.058
Burcu Uner, Meltem Ezgi Durgun, Samet Ozdemir, Cetin Tas, Melike Uner, Yildiz Ozsoy
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Abstract

Ocular drug delivery methods are highly favored for boosting bioavailability, patient compliance, and lower adverse effects and dose frequency. In addition to preventing adverse effects from the active ingredient, the parts of drug delivery systems must be nontoxic and nonallergic as well. Mitochondrial toxicity test (MTT) and Hen's egg chorioallantois membrane (HET-CAM) assay are the most often utilized tests based on this dilemma. The toxicity of loteprednol etabonate loaded solid lipid nanoparticles, lipid nanostructured carriers, and nanoemulsion were compared. Oleic acid, Precirol®ATO5, and Pluronic® F68 were used in the preparation. Their toxicities were evaluated by using two different toxicity tests (MTT and HET-CAM). The results suggest that there are no significant differences between the HET-CAM and MTT assays. It is noteworthy that the HET-CAM assay offers a more cost-effective and environmentally friendly alternative to the MTT assay, as it does not require cell culture and generates less toxic waste. This information may be useful to consider when selecting between the two assays.

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通过比较两种不同的毒性生物测定法测定眼部给药系统的毒性偏好。
眼部给药方法在提高生物利用度、患者依从性、降低不良反应和剂量频率方面备受青睐。除了防止活性成分的不良反应外,给药系统的各部分也必须无毒和无过敏性。线粒体毒性试验(MTT)和母鸡绒毛尿囊膜(HET-CAM)是基于这一困境最常用的试验。比较了负载洛替普诺的固体脂质纳米颗粒、脂质纳米结构载体和纳米乳液的毒性。制备过程中使用了油酸、Precisrol®ATO5和Pluronic®F68。通过两种不同的毒性试验(MTT和HET-CAM)评估它们的毒性。结果表明,HET-CAM和MTT检测之间没有显著差异。值得注意的是,HET-CAM测定法为MTT测定法提供了一种更具成本效益和环境友好的替代方法,因为它不需要细胞培养,产生的毒性废物更少。当在两种测定之间进行选择时,该信息可能是有用的。
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来源期刊
Assay and drug development technologies
Assay and drug development technologies 医学-生化研究方法
CiteScore
3.60
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: ASSAY and Drug Development Technologies provides access to novel techniques and robust tools that enable critical advances in early-stage screening. This research published in the Journal leads to important therapeutics and platforms for drug discovery and development. This reputable peer-reviewed journal features original papers application-oriented technology reviews, topical issues on novel and burgeoning areas of research, and reports in methodology and technology application. ASSAY and Drug Development Technologies coverage includes: -Assay design, target development, and high-throughput technologies- Hit to Lead optimization and medicinal chemistry through preclinical candidate selection- Lab automation, sample management, bioinformatics, data mining, virtual screening, and data analysis- Approaches to assays configured for gene families, inherited, and infectious diseases- Assays and strategies for adapting model organisms to drug discovery- The use of stem cells as models of disease- Translation of phenotypic outputs to target identification- Exploration and mechanistic studies of the technical basis for assay and screening artifacts
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