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Multi-Responsive Molecularly Imprinted Polymer Nanocapsules as Biological Environment-Adaptable Drug Carriers for
Huiqi Zhang1, Yanyan Mu1, Chaoyue Han1
1State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Functional Polymer Materials (Ministry of Education), and College of Chemistry, Nankai University, Tianjin, 300071, China.
Researchers developed smart polymer nanocapsules for targeted cancer therapy. These adaptable nanocarriers overcome biological barriers, deliver drugs on-demand to tumor cells, and significantly inhibit tumor growth in mice.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Polymer Chemistry
Background:
- Developing adaptable nanocarriers for targeted cancer therapy is challenging.
- Existing systems struggle to overcome biological barriers and achieve on-demand drug delivery to tumor cells.
Purpose of the Study:
- To synthesize multi-responsive, hydrophilic, fluorescent molecularly imprinted polymer (MIP) nanocapsules for enhanced cancer therapy.
- To create a versatile nanoplatform for on-demand drug delivery and tumor inhibition.
Main Methods:
- Synthesized disulfide-crosslinked fluorescent MIP nanocapsules with sialic acid-imprinted sites.
- Incorporated thermo/pH-responsive block copolymer brushes and poly(methacrylic acid) chains.
- Evaluated drug loading, release kinetics, biocompatibility, and in vivo antitumor efficacy.
Main Results:
- Achieved ultrahigh drug loading capacity (688 µmol g⁻¹) with minimal premature release.
- Demonstrated tumor-microenvironment-triggered polymer brush detachment and charge reversal.
- Showcased prolonged circulation, specific tumor accumulation, enhanced penetration, and rapid intracellular drug release.
- Significantly inhibited tumor growth in mouse models.
Conclusions:
- The developed MIP nanocapsules offer a promising "all-in-one" drug delivery system for cancer therapy.
- This versatile nanoplatform enables tailored drug loading for various cancer treatment strategies.
- The smart nanocarriers demonstrate efficient overcoming of biological barriers and targeted tumor cell delivery.
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