Aptamer-Functionalized Liposome Delivery System Based on Multifunctional Microreactor Design

Breast cancer remains the leading cause of cancer-related mortality in women, with conventional chemotherapy often limited by systemic toxicity due to poor drug targeting. Here, we present an integrated microfluidic chip (MMLP) that enables one-step integrated postprocessing, including solvent removal and ligand conjugation. The MMLP chip combines Y-shaped, crescent-shaped, U-shaped, and Tesla-type microchannels, augmented with pillar arrays to enhance mixing efficiency at low flow rates. A dedicated third channel allows simultaneous solvent removal and aptamer conjugation. Through computational fluid dynamics (CFD) simulations, we optimized the flow-rate ratio (lipid phase/aqueous phase/postprocessing phase = 1:5:2) and achieved AS1411 aptamer modification via thiol-maleimide chemistry. The resulting AS1411 aptamer-functionalized liposomes loaded with doxorubicin (D@Lip-Apt) exhibited uniform size (155 ± 3.2 nm, PDI = 0.17) and high drug encapsulation efficiency (76.64 ± 0.52%). In vitro and in vivo studies confirmed the nanoparticles' superior stability and tumor-targeting specificity. This modular microreactor offers exceptional flexibility in tailoring liposome properties for breast cancer therapy and demonstrates scalability for industrial production through dimensional or parallel amplification.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2026-06-24
DOI
https://doi.org/10.1021/acsami.6c09467
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
Field-Weighted Citation Impact
0.00

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article

Aptamer-Functionalized Liposome Delivery System Based on Multifunctional Microreactor Design

Wenjin Chen, Dengyue Chen, Bing Wang, Jiaqi Guo et al.
ACS Applied Materials & Interfaces
Nanoparticle-Based Drug Delivery
article

Aptamer-Functionalized Liposome Delivery System Based on Multifunctional Microreactor Design

Wenjin Chen, Dengyue Chen, Bing Wang, Jiaqi Guo, Yannan Wu, Yueyao Lin, Shanshan Peng, Ruiji Lin
article en

Abstract

Breast cancer remains the leading cause of cancer-related mortality in women, with conventional chemotherapy often limited by systemic toxicity due to poor drug targeting. Here, we present an integrated microfluidic chip (MMLP) that enables one-step integrated postprocessing, including solvent removal and ligand conjugation. The MMLP chip combines Y-shaped, crescent-shaped, U-shaped, and Tesla-type microchannels, augmented with pillar arrays to enhance mixing efficiency at low flow rates. A dedicated third channel allows simultaneous solvent removal and aptamer conjugation. Through computational fluid dynamics (CFD) simulations, we optimized the flow-rate ratio (lipid phase/aqueous phase/postprocessing phase = 1:5:2) and achieved AS1411 aptamer modification via thiol-maleimide chemistry. The resulting AS1411 aptamer-functionalized liposomes loaded with doxorubicin (D@Lip-Apt) exhibited uniform size (155 ± 3.2 nm, PDI = 0.17) and high drug encapsulation efficiency (76.64 ± 0.52%). In vitro and in vivo studies confirmed the nanoparticles' superior stability and tumor-targeting specificity. This modular microreactor offers exceptional flexibility in tailoring liposome properties for breast cancer therapy and demonstrates scalability for industrial production through dimensional or parallel amplification.

ACS Applied Materials & Interfaces
Target (United States) (US), Changsha Medical University (CN), Xiamen University (CN), Nankai University (CN), Kochi Medical School Hospital (JP), Fifth Hospital of Shijiazhuang (CN), Nuclear and Radiation Safety Center (CN), Center for Translational Molecular Medicine (NL)
National Natural Science Foundation of China, Natural Science Foundation of Fujian Province, Fujian Provincial Department of Science and Technology, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 13%
Nanoparticle-Based Drug Delivery
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