Department of Pharmacy and BioTechnology, PharmTech Lab, University of Bologna, Via S. Donato 19/2, 40127 Bologna, Italy.
Department of Pharmacy and BioTechnology, PharmTech Lab, University of Bologna, Via S. Donato 19/2, 40127 Bologna, Italy.
Eur J Pharm Biopharm. 2018 Nov;132:1-10. doi: 10.1016/j.ejpb.2018.08.014. Epub 2018 Aug 31.
Oral local delivery of therapeutic biologics is generally limited due to the multiple obstacles of the gastrointestinal (GI) tract, mainly represented by acidic stomach pH and digestive enzymes. In the present study, spray congealing was used to prepare solid lipid microparticles (SLMs) loaded with β-galactosidase (lactase), an enzyme used for the treatment of lactose intolerance, to achieve a local drug delivery to the small intestine. Lactase was characterized in terms of activity at different pH, kinetic parameters and proteolytic degradation by digestive enzymes. Then, five lipid excipients were used to prepare unloaded SLMs, which were tested regarding lipase-induced digestion. The lipid with the best performance (glyceryl trimyristate) was used to prepare lactase-loaded SLMs. Spray congealed SLMs were spherical with very good encapsulation efficiency (>95%). The ability of the SLMs to protect the enzyme from the degradation in gastric environment was correlated with the particle size and the best formulation preserved the lactase activity up to 70%. Lactase was promptly released in simulated intestinal environment, and an in vitro positive food effect was observed. The present study demonstrated the potential of spray congealing for the preparation of solid lipid formulations able to achieve local oral delivery of a biologic drug.
由于胃肠道(GI)的多种障碍,包括酸性胃 pH 值和消化酶,治疗性生物制剂的口服局部递送通常受到限制。在本研究中,喷雾凝固法被用于制备负载β-半乳糖苷酶(乳糖酶)的固体脂质微粒(SLM),乳糖酶是一种用于治疗乳糖不耐受的酶,以实现对小肠的局部药物递送。从不同 pH 值下的活性、动力学参数和消化酶的蛋白水解降解等方面对乳糖酶进行了表征。然后,使用五种脂质赋形剂制备未负载的 SLM,并对其进行了脂酶诱导消化测试。性能最佳的脂质(三硬脂精)用于制备负载乳糖酶的 SLM。喷雾凝固 SLM 呈球形,具有非常好的包封效率(>95%)。SLM 保护酶免受胃环境中降解的能力与粒径相关,最佳配方可将乳糖酶活性保持在 70%以上。乳糖酶在模拟肠道环境中迅速释放,并观察到体外阳性食物效应。本研究证明了喷雾凝固法制备能够实现生物药物局部口服递送的固体脂质制剂的潜力。