Pyridine-appended disulfidephospholipids enable exceptionally high drug loading and stability as a robust liposomal platform

Abstract

Low drug loading and instability of liposomes are two main challenges in the clinic. Herein, a liposomal platform from alternative pyridine-appended disulfidephospholipid (Pyr-SS-PC) was developed for delivering camptothecin (CPT) with high loading and stability. These Pyr-SS-PC lipids with π–π stacking open a general gate in the delivery of aromatic ring-containing drugs.