Oral absorption and lymphatic transport of baicalein following drug–phospholipid complex incorporation in self-microemulsifying drug delivery systems
Hengfeng Liao1,2, Yue Gao1,2, Chunfang Lian1,2, Yun Zhang1,2, Bangyuan Wang1,2, Yanfang Yang1,2, Jun Ye1,2, Yu Feng1,2, Yuling Liu1,2 1State Key Laboratory of Bioactive substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Unio...
Guardado en:
| Autores principales: | , , , , , , , , |
|---|---|
| Formato: | article |
| Lenguaje: | EN |
| Publicado: |
Dove Medical Press
2019
|
| Materias: | |
| Acceso en línea: | https://doaj.org/article/1dac03829f654d858baa268c22a6bd5b |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
| id |
oai:doaj.org-article:1dac03829f654d858baa268c22a6bd5b |
|---|---|
| record_format |
dspace |
| spelling |
oai:doaj.org-article:1dac03829f654d858baa268c22a6bd5b2021-12-02T10:50:21ZOral absorption and lymphatic transport of baicalein following drug–phospholipid complex incorporation in self-microemulsifying drug delivery systems1178-2013https://doaj.org/article/1dac03829f654d858baa268c22a6bd5b2019-09-01T00:00:00Zhttps://www.dovepress.com/oral-absorption-and-lymphatic-transport-of-baicalein-following-drug-ph-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Hengfeng Liao1,2, Yue Gao1,2, Chunfang Lian1,2, Yun Zhang1,2, Bangyuan Wang1,2, Yanfang Yang1,2, Jun Ye1,2, Yu Feng1,2, Yuling Liu1,2 1State Key Laboratory of Bioactive substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, People’s Republic of China; 2Beijing Key Laboratory of Drug Delivery Technology and Novel Formulation, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, People’s Republic of ChinaCorrespondence: Yuling LiuState Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, 1 Xiannongtan Street, Beijing 100050, People’s Republic of ChinaTel +86 108 928 5188Fax +86 108 928 5190Email ylliu@imm.ac.cnPurpose: The aims of this study were to prepare a baicalein self-microemulsion with baicalein-phospholipid complex as the intermediate (BAPC-SMEDDS) and to compare its effects with those of conventional baicalein self-microemulsion (CBA-SMEDDS) on baicalein oral absorption and lymphatic transport.Methods: Two SMEDDS were characterized by emulsifying efficiency, droplet size, zeta potential, cloud point, dilution stability, physical stability, and in vitro release and lipolysis. Different formulations of 40 mg/kg baicalein were orally administered to Sprague-Dawley rats to investigate their respective bioavailabilities. The chylomicron flow blocking rat model was used to evaluate their lymphatic transport.Results: The droplet sizes of BAPC-SMEDDS and CBA-SMEDDS after 100x dilution were 9.6±0.2 nm and 11.3±0.4 nm, respectively. In vivo experiments indicated that the relative bioavailability of CBA-SMEDDS and BAPC-SMEDDS was 342.5% and 448.7% compared to that of free baicalein (BA). The AUC0–t and Cmax of BAPC-SMEDDS were 1.31 and 1.87 times higher than those of CBA-SMEDDS, respectively. The lymphatic transport study revealed that 81.2% of orally absorbed BA entered the circulation directly through the portal vein, whereas approximately 18.8% was transported into the blood via lymphatic transport. CBA-SMEDDS and BAPC-SMEDDS increased the lymphatic transport ratio of BA from 18.8% to 56.2% and 70.2%, respectively. Therefore, self-microemulsion not only significantly improves oral bioavailability of baicalein, but also increases the proportion lymphatically transported. This is beneficial to the direct interaction of baicalein with relevant immune cells in the lymphatic system and for proper display of its effects.Conclusion: This study demonstrates the oral absorption and lymphatic transport characteristics of free baicalein and baicalein SMEDDS with different compositions. This is of great significance to studies on lymphatic targeted delivery of natural immunomodulatory compounds.Keywords: SMEDDS, phospholipid complex, baicalein, oral bioavailability, lymphatic transportLiao HGao YLian CZhang YWang BYang YYe JFeng YLiu YDove Medical PressarticleSMEDDSphospholipid complexbaicaleinoral bioavailabilitylymphatic transportMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 14, Pp 7291-7306 (2019) |
| institution |
DOAJ |
| collection |
DOAJ |
| language |
EN |
| topic |
SMEDDS phospholipid complex baicalein oral bioavailability lymphatic transport Medicine (General) R5-920 |
| spellingShingle |
SMEDDS phospholipid complex baicalein oral bioavailability lymphatic transport Medicine (General) R5-920 Liao H Gao Y Lian C Zhang Y Wang B Yang Y Ye J Feng Y Liu Y Oral absorption and lymphatic transport of baicalein following drug–phospholipid complex incorporation in self-microemulsifying drug delivery systems |
| description |
Hengfeng Liao1,2, Yue Gao1,2, Chunfang Lian1,2, Yun Zhang1,2, Bangyuan Wang1,2, Yanfang Yang1,2, Jun Ye1,2, Yu Feng1,2, Yuling Liu1,2 1State Key Laboratory of Bioactive substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, People’s Republic of China; 2Beijing Key Laboratory of Drug Delivery Technology and Novel Formulation, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, People’s Republic of ChinaCorrespondence: Yuling LiuState Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, 1 Xiannongtan Street, Beijing 100050, People’s Republic of ChinaTel +86 108 928 5188Fax +86 108 928 5190Email ylliu@imm.ac.cnPurpose: The aims of this study were to prepare a baicalein self-microemulsion with baicalein-phospholipid complex as the intermediate (BAPC-SMEDDS) and to compare its effects with those of conventional baicalein self-microemulsion (CBA-SMEDDS) on baicalein oral absorption and lymphatic transport.Methods: Two SMEDDS were characterized by emulsifying efficiency, droplet size, zeta potential, cloud point, dilution stability, physical stability, and in vitro release and lipolysis. Different formulations of 40 mg/kg baicalein were orally administered to Sprague-Dawley rats to investigate their respective bioavailabilities. The chylomicron flow blocking rat model was used to evaluate their lymphatic transport.Results: The droplet sizes of BAPC-SMEDDS and CBA-SMEDDS after 100x dilution were 9.6±0.2 nm and 11.3±0.4 nm, respectively. In vivo experiments indicated that the relative bioavailability of CBA-SMEDDS and BAPC-SMEDDS was 342.5% and 448.7% compared to that of free baicalein (BA). The AUC0–t and Cmax of BAPC-SMEDDS were 1.31 and 1.87 times higher than those of CBA-SMEDDS, respectively. The lymphatic transport study revealed that 81.2% of orally absorbed BA entered the circulation directly through the portal vein, whereas approximately 18.8% was transported into the blood via lymphatic transport. CBA-SMEDDS and BAPC-SMEDDS increased the lymphatic transport ratio of BA from 18.8% to 56.2% and 70.2%, respectively. Therefore, self-microemulsion not only significantly improves oral bioavailability of baicalein, but also increases the proportion lymphatically transported. This is beneficial to the direct interaction of baicalein with relevant immune cells in the lymphatic system and for proper display of its effects.Conclusion: This study demonstrates the oral absorption and lymphatic transport characteristics of free baicalein and baicalein SMEDDS with different compositions. This is of great significance to studies on lymphatic targeted delivery of natural immunomodulatory compounds.Keywords: SMEDDS, phospholipid complex, baicalein, oral bioavailability, lymphatic transport |
| format |
article |
| author |
Liao H Gao Y Lian C Zhang Y Wang B Yang Y Ye J Feng Y Liu Y |
| author_facet |
Liao H Gao Y Lian C Zhang Y Wang B Yang Y Ye J Feng Y Liu Y |
| author_sort |
Liao H |
| title |
Oral absorption and lymphatic transport of baicalein following drug–phospholipid complex incorporation in self-microemulsifying drug delivery systems |
| title_short |
Oral absorption and lymphatic transport of baicalein following drug–phospholipid complex incorporation in self-microemulsifying drug delivery systems |
| title_full |
Oral absorption and lymphatic transport of baicalein following drug–phospholipid complex incorporation in self-microemulsifying drug delivery systems |
| title_fullStr |
Oral absorption and lymphatic transport of baicalein following drug–phospholipid complex incorporation in self-microemulsifying drug delivery systems |
| title_full_unstemmed |
Oral absorption and lymphatic transport of baicalein following drug–phospholipid complex incorporation in self-microemulsifying drug delivery systems |
| title_sort |
oral absorption and lymphatic transport of baicalein following drug–phospholipid complex incorporation in self-microemulsifying drug delivery systems |
| publisher |
Dove Medical Press |
| publishDate |
2019 |
| url |
https://doaj.org/article/1dac03829f654d858baa268c22a6bd5b |
| work_keys_str_mv |
AT liaoh oralabsorptionandlymphatictransportofbaicaleinfollowingdrugndashphospholipidcomplexincorporationinselfmicroemulsifyingdrugdeliverysystems AT gaoy oralabsorptionandlymphatictransportofbaicaleinfollowingdrugndashphospholipidcomplexincorporationinselfmicroemulsifyingdrugdeliverysystems AT lianc oralabsorptionandlymphatictransportofbaicaleinfollowingdrugndashphospholipidcomplexincorporationinselfmicroemulsifyingdrugdeliverysystems AT zhangy oralabsorptionandlymphatictransportofbaicaleinfollowingdrugndashphospholipidcomplexincorporationinselfmicroemulsifyingdrugdeliverysystems AT wangb oralabsorptionandlymphatictransportofbaicaleinfollowingdrugndashphospholipidcomplexincorporationinselfmicroemulsifyingdrugdeliverysystems AT yangy oralabsorptionandlymphatictransportofbaicaleinfollowingdrugndashphospholipidcomplexincorporationinselfmicroemulsifyingdrugdeliverysystems AT yej oralabsorptionandlymphatictransportofbaicaleinfollowingdrugndashphospholipidcomplexincorporationinselfmicroemulsifyingdrugdeliverysystems AT fengy oralabsorptionandlymphatictransportofbaicaleinfollowingdrugndashphospholipidcomplexincorporationinselfmicroemulsifyingdrugdeliverysystems AT liuy oralabsorptionandlymphatictransportofbaicaleinfollowingdrugndashphospholipidcomplexincorporationinselfmicroemulsifyingdrugdeliverysystems |
| _version_ |
1718396574975918080 |