Photopolymerized Micelle-Laden Hydrogels Can Simultaneously Form and Encapsulate Nanocrystals to Improve Drug Substance Solubility and Expedite Drug Product Design

被引:27
作者
Godfrin, Paul Douglas [1 ]
Lee, Hyundo [1 ]
Lee, Ji Hyun [1 ]
Doyle, Patrick S. [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
基金
新加坡国家研究基金会;
关键词
hydrogels; hydrophobic drugs; micelles; nanocrystals; solubility; ACTIVE PHARMACEUTICAL INGREDIENTS; COMPOSITE HYDROGELS; DELIVERY-SYSTEMS; ORAL ABSORPTION; RELEASE; NANOSUSPENSIONS; NANOMEDICINES; DISSOLUTION; POLYMERS; BIOAVAILABILITY;
D O I
10.1002/smll.201803372
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Formulation technologies are critical for increasing the efficacy of drug products containing poorly soluble hydrophobic drugs, which compose roughly 70% of small molecules in commercial pipelines. Nanomedicines, such as nanocrystal formulations and amorphous solid suspensions, are effective approaches to increasing solubility. However, existing techniques require additional processing into a final dosage form, which strongly influences drug delivery and clinical performance. To enhance hydrophobic drug product efficacy and clinical throughput, a hydrogel material is developed as a sacrificial template to simultaneously form and encapsulate nanocrystals. These hydrogels contain micelles chemically bound to the hydrogel matrix, where the surfactant structure dictates the crystal size and drug loading. Therefore, nanocrystals can be produced in high yield (up to 90% drug loading, by weight) with precisely controlled sizes as small as 4 nm independently of hydrogel composition. Nanocrystals and surfactant are then released together to increase the solubility up to 70 times above bulk crystalline material. By integrating nanocrystals into a final dosage form, micelle-laden hydrogels simplify hydrophobic drug product design.
引用
收藏
页数:14
相关论文
共 78 条
[1]   Mucoadhesive polymeric platforms for controlled drug delivery [J].
Andrews, Gavin P. ;
Laverty, Thomas P. ;
Jones, David S. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2009, 71 (03) :505-518
[2]   Solubility Advantage of Amorphous Drugs and Pharmaceutical Cocrystals [J].
Babu, N. Jagadeesh ;
Nangia, Ashwini .
CRYSTAL GROWTH & DESIGN, 2011, 11 (07) :2662-2679
[3]   Core-Shell Composite Hydrogels for Controlled Nanocrystal Formation and Release of Hydrophobic Active Pharmaceutical Ingredients [J].
Badruddoza, Abu Zayed Md ;
Godfrin, P. Douglas ;
Myerson, Allan S. ;
Trout, Bernhardt L. ;
Doyle, Patrick S. .
ADVANCED HEALTHCARE MATERIALS, 2016, 5 (15) :1960-1968
[4]   BDDCS Applied to Over 900 Drugs [J].
Benet, Leslie Z. ;
Broccatelli, Fabio ;
Oprea, Tudor I. .
AAPS JOURNAL, 2011, 13 (04) :519-547
[5]   Solubilization capabilities of some cationic, anionic, and nonionic surfactants toward the poorly water-soluble antibiotic drug erythromycin [J].
Bhat, Parvaiz Ahmad ;
Dar, Aijaz Ahmad ;
Rather, Ghulam Mohammad .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2008, 53 (06) :1271-1277
[6]  
Bromberg Lev, 2005, Expert Opin Drug Deliv, V2, P1003, DOI 10.1517/17425247.2.6.1003
[7]   Thermoresponsive polymers as gene and drug delivery vectors: architecture and mechanism of action [J].
Calejo, Maria Teresa ;
Sande, Sverre Arne ;
Nystrom, Bo .
EXPERT OPINION ON DRUG DELIVERY, 2013, 10 (12) :1669-1686
[8]   Application of formulation technologies in lead candidate selection and optimization [J].
Chaubal, MV .
DRUG DISCOVERY TODAY, 2004, 9 (14) :603-609
[9]   A Brief Literature and Patent Review of Nanosuspensions to a Final Drug Product [J].
Chin, William Wei Lim ;
Parmentier, Johannes ;
Widzinski, Michael ;
Tan, En Hui ;
Gokhale, Rajeev .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2014, 103 (10) :2980-2999
[10]   Self-assembled and nanostructured hydrogels for drug delivery and tissue engineering [J].
Chung, Hyun Jung ;
Park, Taie Gwan .
NANO TODAY, 2009, 4 (05) :429-437