The Fabrication, Drug Loading, and Release Behavior of Porous Mannitol.

PVP K30 adsorption kinetics co-spray–antisolvent dissolution behavior mechanism porous mannitol

Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
04 Feb 2024
Historique:
received: 30 12 2023
revised: 21 01 2024
accepted: 29 01 2024
medline: 10 2 2024
pubmed: 10 2 2024
entrez: 10 2 2024
Statut: epublish

Résumé

Porous materials are widely used as an effective strategy for the solubilization of insoluble drugs. In order to improve the solubility and bioavailability of low water-solubility drugs, it is necessary to prepare porous materials. Mannitol is one of the most popular excipients in food and drug formulations. In this study, porous mannitol was investigated as a drug carrier for low water solubility drugs. Its fabrication, drug loading, and drug release mechanisms were investigated. Porous mannitol was fabricated using the co-spray-antisolvent process and utilizing polyvinylpyrrolidone K30 (PVP K30) as the template agent. Porous mannitol particles were prepared by changing the proportion of the template agent, spraying the particles with mannitol, and eluting with ethanol in order to regulate their pore structure. In subsequent studies, porous mannitol morphology and characteristics were determined systematically. Furthermore, curcumin and ibuprofen, two poorly water-soluble drugs, were loaded into porous mannitol, and their release profiles were analyzed. The results of the study indicated that porous mannitol can be prepared using PVP K30 as a template and that the amount of template agent can be adjusted in order to control the structure of the porous mannitol. When the template agent was added in amounts of 1%, 3%, and 5%, the mannitol pore size increased by 167.80%, 95.16%, and 163.98%, respectively, compared to raw mannitol. Molecular docking revealed that mannitol and drugs are adsorbents and adhere to each other by force interaction. The cumulative dissolution of curcumin and ibuprofen-loaded porous mannitol reached 69% and 70%, respectively. The release mechanism of curcumin and ibuprofen from drug-loaded mannitol was suitable for the Korsmeyer-Peppas kinetic model. In summary, the co-spray-antisolvent method proved effective in fabricating porous materials rapidly, and porous mannitol had a remarkable effect on drug solubilization. The results obtained are conducive to the development of porous materials.

Identifiants

pubmed: 38338458
pii: molecules29030715
doi: 10.3390/molecules29030715
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : the National Natural Science Foundation of China
ID : the National Natural Science Foundation of China
Organisme : the National Natural Science Foundation of China
ID : 82360777
Organisme : China Postdoctoral Science Foundation
ID : 2019M662278
Organisme : National Natural Science Foundation of Jiangxi Province
ID : 20202BAB216039
Organisme : National Natural Science Foundation of Jiangxi Province
ID : 20232ACB216015
Organisme : National Natural Science Foundation of Jiangxi Province
ID : 20212BAB216009
Organisme : National Natural Science Foundation of Jiangxi Province
ID : 20232BAB206166
Organisme : 2020-2022 Young Talents Support Project of Chinese Society of Chinese Medicine
ID : 2020-QNRC2-07
Organisme : Jiangxi University of Chinese Medicine Science and Technology Innovation Team Development Program
ID : CXTD-22004
Organisme : Program of Jiangxi University of Chinese Medicine
ID : 2021BSZR015
Organisme : Program of Jiangxi University of Chinese Medicine
ID : 2022BSZR003
Organisme : and Training Plan for Academic and Technical Leaders of Major Disciplines In Jiangxi Province
ID : 20204BCJL22048

Auteurs

Zhe Li (Z)

Key Laboratory of Modern Preparation of TCM of Ministry of Education, Institute for Advanced Study, Jiangxi University of Chinese Medicine, Nanchang 330004, China.

Xiaosui Luo (X)

Key Laboratory of Modern Preparation of TCM of Ministry of Education, Institute for Advanced Study, Jiangxi University of Chinese Medicine, Nanchang 330004, China.

Qiong Li (Q)

Key Laboratory of Modern Preparation of TCM of Ministry of Education, Institute for Advanced Study, Jiangxi University of Chinese Medicine, Nanchang 330004, China.

Zhengji Jin (Z)

Key Laboratory of Modern Preparation of TCM of Ministry of Education, Institute for Advanced Study, Jiangxi University of Chinese Medicine, Nanchang 330004, China.

Abid Naeem (A)

Key Laboratory of Modern Preparation of TCM of Ministry of Education, Institute for Advanced Study, Jiangxi University of Chinese Medicine, Nanchang 330004, China.

Weifeng Zhu (W)

Key Laboratory of Modern Preparation of TCM of Ministry of Education, Institute for Advanced Study, Jiangxi University of Chinese Medicine, Nanchang 330004, China.

Lihua Chen (L)

Key Laboratory of Modern Preparation of TCM of Ministry of Education, Institute for Advanced Study, Jiangxi University of Chinese Medicine, Nanchang 330004, China.

Yi Feng (Y)

Key Laboratory of Modern Preparation of TCM of Ministry of Education, Institute for Advanced Study, Jiangxi University of Chinese Medicine, Nanchang 330004, China.
Engineering Research Center of Modern Preparation Technology of TCM of Ministry of Education, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.

Liangshan Ming (L)

Key Laboratory of Modern Preparation of TCM of Ministry of Education, Institute for Advanced Study, Jiangxi University of Chinese Medicine, Nanchang 330004, China.

Classifications MeSH