Folic acid antibody-targeted nanoliposomes encapsulating vincristine efficiently inhibit the growth of gastric cancer cells

Gastric cancer (GC) remains challenging to treat clinically owing to poor tumortargeting performance, systemic toxicity and frequent chemoresistance. Herein, we constructed folic acidantibody(FA)functionalized vincristineloaded nanoliposomes (FAVCRMLs) for targeted gastric cancer therapy. The spherical nanoparticles had a mean size of 241.47.6nm and zeta potential of 38.57.9mV, with encapsulation efficiency of 93.720.48% and drugloading content of 10.370.69%. Approximately 88% of vincristine was released under acidic conditions in a pHdependent manner. These liposomes exhibited satisfactory biocompatibility and enhanced cellular uptake in GC cells relative to free vincristine and nontargeted VCRMLs. Invivo assays showed an 85% tumorsuppression rate, 9% of tumorbearing nude mice survived by day 71. In summary, FAVCRMLs represent an effective targeted nanotherapeutic agent against gastric cancer.

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Publication Details

Journal
Nano LIFE
Published
2026-10-30
DOI
https://doi.org/10.1142/s1793984427500073
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
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article

Folic acid antibody-targeted nanoliposomes encapsulating vincristine efficiently inhibit the growth of gastric cancer cells

Xianting Jin, Zhouhui Jin, Yiwen Cui, Huan Liu et al.
2 links
Nano LIFE
Nanoparticle-Based Drug Delivery
article

Folic acid antibody-targeted nanoliposomes encapsulating vincristine efficiently inhibit the growth of gastric cancer cells

Xianting Jin, Zhouhui Jin, Yiwen Cui, Huan Liu, Long Qin, Yunping Guo, Shuiying Wang, Lin Wang
article en

Abstract

Gastric cancer (GC) remains challenging to treat clinically owing to poor tumortargeting performance, systemic toxicity and frequent chemoresistance. Herein, we constructed folic acidantibody(FA)functionalized vincristineloaded nanoliposomes (FAVCRMLs) for targeted gastric cancer therapy. The spherical nanoparticles had a mean size of 241.47.6nm and zeta potential of 38.57.9mV, with encapsulation efficiency of 93.720.48% and drugloading content of 10.370.69%. Approximately 88% of vincristine was released under acidic conditions in a pHdependent manner. These liposomes exhibited satisfactory biocompatibility and enhanced cellular uptake in GC cells relative to free vincristine and nontargeted VCRMLs. Invivo assays showed an 85% tumorsuppression rate, 9% of tumorbearing nude mice survived by day 71. In summary, FAVCRMLs represent an effective targeted nanotherapeutic agent against gastric cancer.

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Nanoparticle-Based Drug Delivery
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Folic acid antibody-targeted nanoliposomes encapsulating vincristine efficiently inhibit the growth of gastric cancer cells — Xianting Jin, Zhouhui Jin, et al. · Nano LIFE (2026) | TGRS Research Map | TGRS