Amphiphilic Block Copolymer Nanostructures as a Tunable Delivery Platform: Perspective and Framework for the Future Drug Product Development

被引:12
|
作者
Sinsinbar, Gaurav [1 ]
Bindra, Anivind Kaur [1 ]
Liu, Shaoqiong [1 ]
Chia, Teck Wan [1 ]
Yoong Eng, Eunice Chia [1 ]
Loo, Ser Yue [1 ]
Lam, Jian Hang [1 ]
Schultheis, Katherine [1 ]
Nallani, Madhavan [1 ]
机构
[1] ACM Biolabs Pte Ltd, Singapore 638075, Singapore
关键词
MESSENGER-RNA; IN-VITRO; BIODEGRADABLE POLYMERSOMES; DENDRITIC CELLS; CHAIN-LENGTH; INTRACELLULAR DELIVERY; LIPID NANOPARTICLES; CONTROLLED-RELEASE; CROSS-PRESENTATION; PHAGOCYTIC UPTAKE;
D O I
10.1021/acs.biomac.3c00858
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nanoformulation of active payloads or pharmaceutical ingredients (APIs) has always been an area of interest to achieve targeted, sustained, and efficacious delivery. Various delivery platforms have been explored, but loading and delivery of APIs have been challenging because of the chemical and structural properties of these molecules. Polymersomes made from amphiphilic block copolymers (ABCPs) have shown enormous promise as a tunable API delivery platform and confer multifold advantages over lipid-based systems. For example, a COVID booster vaccine comprising polymersomes encapsulating spike protein (ACM-001) has recently completed a Phase I clinical trial and provides a case for developing safe drug products based on ABCP delivery platforms. However, several limitations need to be resolved before they can reach their full potential. In this Perspective, we would like to highlight such aspects requiring further development for translating an ABCP-based delivery platform from a proof of concept to a viable commercial product.
引用
收藏
页码:541 / 563
页数:23
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