啮齿动物饮食中加入活体生物治疗产品(LBP):一种创新的给药策略,以支持LBP干预的临床前动物研究

IF 3.4 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Haixi Cui, Yongrong Zhang, Hua Yu, R. Gary Hollenbeck, Lydia Nyasae, Yihan Wang, Yiguang Han, Zhiyong Yang, Hanping Feng, Stephen W. Hoag
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引用次数: 0

摘要

目前,在基于动物的临床前研究中,活体生物治疗产品(lbp)的给药是通过口服灌胃或通过供水自愿消耗来实现的。口服灌胃为实验动物给药提供了最准确和精确的剂量;然而,它会引起应激反应,而且是劳动密集型的,特别是在需要长期给药的情况下,给实验室人员和实验动物都带来了沉重的负担。另一方面,通过供水自愿消耗LBP需要较少的努力和减少动物的应激,但仍然存在一些挑战,如不受控制的剂量,在给药期间LBP活力的变化,由于LBP沉积而导致的剂量不均匀,以及由于水环境中的稳定性和活力问题而需要频繁的补充。为了解决这些问题,我们开发了含有稳定的生物工程益生菌酵母药物(BioPYM™)的冻干啮齿动物饮食颗粒,具有可定制的颗粒大小,强大的机械强度,低易碎性,均匀的BioPYM分布,并且在4至8°C的储存条件下具有10周的稳定性,确保易于处理和更可靠的给药。通过对冻干保护剂和混合方法的优化,获得了在干饲料中保存细胞活力的最佳效果。活的BioPYM细胞脱落的药代动力学研究及其治疗有效载荷揭示了靶向啮齿动物胃肠道系统的治疗剂的有效递送。总的来说,biopym -饮食微丸代表了一种改进的方法来传递LBP,并提供方便和精确的剂量。此外,该方法提高了实验动物的福利,减少了实验室的工作量。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rodent Diets Incorporated with Live Biotherapeutic Products (LBPs): An Innovative Dosing Strategy to Support Preclinical Animal Studies on LBP Intervention

Currently, the administration of live biotherapeutic products (LBPs) in animal-based pre-clinical studies is achieved via oral gavage or voluntary consumption through the water supply. Oral gavage provides the most accurate and precise dosing for the administration of LBPs to laboratory animals; however, it induces stress responses and is labor-intensive, especially when long-term dosing is needed, placing a significant burden on both lab personnel and the subject animals. On the other hand, voluntary LBP consumption through water supply requires less effort and reduces animal stress, but still puts challenges concerning uncontrolled dosing, variations in LBP viability during the dosing period, uneven dosing due to sedimentation of LBPs, and the need for frequent refreshments due to stability and viability concerns in an aqueous environment. To address these problems, we developed lyophilized rodent diet pellets incorporated with stabilized Bioengineered Probiotic Yeast Medicines (BioPYM™), with customizable pellet size, robust mechanical strength, low friability, uniform BioPYM distribution, and proved stability for 10 weeks at 4 to 8°C storage, ensuring easy handling and more reliable dosing. Optimal cell viability preservation in dry diets was achieved through optimization of lyoprotectant and blending methods. Pharmacokinetic studies of the shedding of live BioPYM cells and their therapeutic payloads revealed the effective delivery of therapeutic agents targeting rodent gastrointestinal system. Overall, BioPYM-diet pellets represent an improved method for the delivery of LBP, and provide convenient and precise dosing. In addition, this method improves laboratory animal welfare and decreases laboratory workload.

Graphical Abstract

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来源期刊
AAPS PharmSciTech
AAPS PharmSciTech 医学-药学
CiteScore
6.80
自引率
3.00%
发文量
264
审稿时长
2.4 months
期刊介绍: AAPS PharmSciTech is a peer-reviewed, online-only journal committed to serving those pharmaceutical scientists and engineers interested in the research, development, and evaluation of pharmaceutical dosage forms and delivery systems, including drugs derived from biotechnology and the manufacturing science pertaining to the commercialization of such dosage forms. Because of its electronic nature, AAPS PharmSciTech aspires to utilize evolving electronic technology to enable faster and diverse mechanisms of information delivery to its readership. Submission of uninvited expert reviews and research articles are welcomed.
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