A tumor active targeting nano drug delivery system that can reverse tumor drug resistance
A nano-drug delivery system and active targeting technology, which can be used in anti-tumor drugs, drug combinations, anti-infective drugs, etc., and can solve problems such as poor hydrophilicity, low drug loading, and capture
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2017-06-30
- Estimated Expiration
- Not applicable · inactive patent
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Abstract
Description
technical field
[0001] The present invention relates to a prescription composition and application scheme of a tumor active targeting nano drug delivery system capable of reversing drug resistance of tumors. The drug delivery system is a novel lipid mixed polylactic acid-glycolic acid copolymer ( PLGA) nanoparticles. Background technique
[0002] Tumor is a kind of disease that seriously threatens human health. Doxorubicin (DOX) is the first-line drug for tumor chemotherapy, with definite curative effect and low price, but its clinical application is limited by its toxic side effects on normal tissues and easy drug resistance. Therefore, taking doxorubicin as the research object, construct a new drug delivery system with both tumor targeting and acid-sensitivity properties, increase the content of doxorubicin in tumor tissues, reduce its distribution in normal tissues, and reverse drug resistance, and obtain A novel tumor-targeted drug delivery system with high efficiency ...
Examples
Embodiment Construction
[0021] Preparation and antitumor activity of doxorubicin tumor-targeted drug delivery system
[0022] 1 Objective: To evaluate the antitumor activity of DOX-loaded lipid-mixed PLGA nanoparticles.
[0023] 2 Research methods:
[0024] 2.1 Determination of encapsulation efficiency and drug loading
[0025] The nanoparticles were dissolved in DMSO to destroy the nanoparticle structure, and the encapsulation efficiency and drug loading were detected by HPLC-MS / MS.
[0026] Drug loading = (the amount of drug wrapped in the drug delivery system / weight of the drug delivery system) × 100%
[0027] Encapsulation efficiency = (actual drug loading / dosage) × 100%
[0028] 2.2 Evaluation of acid sensitivity characteristics
[0029] The lipid-mixed PLGA nanoparticles were weighed, and the Zeta potential of the lipid-mixed PLGA nanoparticles in different pH (pH 5.0, pH 6.5 and pH 7.4) media was analyzed by laser particle size analyzer.
[0030] 2.3 Cytotoxicity evaluation
[0031] Huma...