Development and Evaluation of a Phospholipid Complex-Loaded SMEDDS for Enhanced Oral Delivery of H007, a Novel Anti-Hyperlipidemic Drug
: H007-PC-SME combines stable phospholipid complex formation with strong self-emulsification performance and effective drug dissolution. By overcoming the intrinsic limitations of the H007 active pharmaceutical ingredient and ordinary H007 tablets, this formulation improves membrane permeability and lymphatic transport, thereby enhancing oral bioavailability and therapeutic potential. The formulation shows good stability and acceptable in vitro biocompatibility under the tested conditions. The preparation process is straightforward, reproducible, and suitable for further pharmaceutical development.
Authors
- Zunsheng Han (ORCID: https://orcid.org/0009-0001-0852-3135)
- Chaoying Liu (ORCID: https://orcid.org/0000-0003-0484-9522)
- Xiaoliang Gong (ORCID: https://orcid.org/0009-0004-6007-2222)
- Chao Zhang (ORCID: https://orcid.org/0000-0003-0399-1201)
- Lie Chen (ORCID: https://orcid.org/0000-0001-9764-4299)
- Jing Feng
- Lundang Guo (ORCID: https://orcid.org/0009-0006-7585-8556)
Institutions
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
Publication Details
- Journal
- Pharmaceutics
- Published
- 2026-04-13
- DOI
- https://doi.org/10.3390/pharmaceutics18040474
- Primary Topic
- Drug Solubulity and Delivery Systems
- Type
- article
- Field-Weighted Citation Impact
- 0.00