Cui Haixi, Zhang Yongrong, Yu Hua, Hollenbeck R Gary, Nyasae Lydia, Wang Yihan, Han Yiguang, Yang Zhiyong, Feng Hanping, Hoag Stephen W
Department of Pharmaceutical Sciences, University of Maryland, Baltimore, Maryland, 21201, USA.
Department of Microbial Pathogenesis, University of Maryland, Baltimore, Maryland, 21201, USA.
AAPS PharmSciTech. 2025 Feb 4;26(2):55. doi: 10.1208/s12249-025-03050-6.
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.
目前,在基于动物的临床前研究中,活生物治疗产品(LBPs)的给药是通过灌胃或通过供水自愿摄取来实现的。灌胃为向实验动物给药LBPs提供了最准确和精确的剂量;然而,它会引发应激反应,且劳动强度大,尤其是在需要长期给药时,给实验室工作人员和实验动物都带来了沉重负担。另一方面,通过供水自愿摄取LBPs所需的工作量较少,且能减轻动物应激,但在给药控制、给药期间LBPs活力变化、由于LBPs沉淀导致的给药不均以及由于水环境中的稳定性和活力问题而需要频繁更换饮水等方面仍存在挑战。为了解决这些问题,我们开发了冻干的啮齿动物饮食颗粒,其中掺入了稳定的生物工程益生菌酵母药物(BioPYM™),其颗粒大小可定制、机械强度高、脆碎度低、BioPYM分布均匀,并在4至8°C储存条件下可稳定保存10周,确保了易于处理和更可靠的给药。通过优化冻干保护剂和混合方法,在干饲料中实现了最佳的细胞活力保存。对活BioPYM细胞及其治疗有效载荷释放的药代动力学研究表明,治疗剂能够有效递送至啮齿动物胃肠道系统。总体而言,BioPYM饮食颗粒代表了一种改进的LBP给药方法,提供了方便且精确的给药方式。此外,这种方法改善了实验动物福利并减少了实验室工作量。