Liposomes are considered the best nanocarrier for delivering
cancer
drugs such as chlorin e6 (Ce6) and paclitaxel (PTX). However, the
poor stability and non-selectivity release of liposomes may severely
limit their further applications. In this study, based on the characteristics
of lutein (L) photo-response and orthoester (OE) acid-response, stable
and dual-responsive liposomes (Dr-lips) have been prepared. The Dr-lips
exhibited a spherical shape with a uniform size of approximately 58.27
nm. Moreover, they displayed a zeta potential ranging from −45.45
to −28.25 mV and showed excellent storage stability, indicating
stable colloidal properties. Additionally, they achieved high drug
encapsulation rates, with 92.27% for PTX and 90.34% for Ce6, respectively.
Meanwhile, under near-infrared (NIR) light at 660 nm, Ce6 plays a
key role in accelerating the photodegradation rate of lutein and PEG-OE-L
while also enhancing tissue penetration ability. Additionally, Dr-lips
loaded with Ce6 and PTX not only displayed excellent pH and photo
dual-responsiveness for targeted delivering and releasing but also
showed remarkable reactive oxygen species (ROS) generation capacity
and impressive anti-tumor activity in vitro. Therefore, it provides
a novel strategy for optimizing stability and enhancing their targeted
drug delivery of liposome.