摘要
The oral delivery of next-generation anti-tuberculosis drugs, such as PBTZ169 and bedaquiline, is hindered by poor solubility and low bioavailability. We have developed a bioinspired delivery platform that combines milk exosomes with PLGA nanoparticles to deliver the two drugs separately. This nano-delivery system leverages the gastrointestinal stability and mucosal penetration of exosomes, along with the high encapsulation efficiency of PLGA, significantly enhancing drug hydrophilicity and stability. In murine models, the exosome-coated nanoparticles increased plasma bioavailability by 2.5–4.9-fold compared to free drugs and achieved superior accumulation in target organs, while mitigating the cardiotoxicity risk associated with BDQ. This synergistic strategy, integrating synthetic and natural carriers, overcomes key pharmacological barriers, offering a promising approach to developing effective and patient-compliant oral therapies for tuberculosis and potentially other infectious diseases.
危险品化学品经营许可证(带存储)