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Research progress in co-delivery of gene and chemotherapy drugs with cationic liposome carrier for cancer therapy / 药学学报
Acta Pharmaceutica Sinica ; (12): 986-992, 2012.
Article in Chinese | WPRIM | ID: wpr-276211
ABSTRACT
Despite recent advances in conventional therapeutic approaches for cancer, the efficacy of chemotherapy for cancer is limited due to the drug resistance and toxic side effects during treatment. To overcome drug resistance, higher doses of the toxic chemotherapy drugs are frequently administered, thus leading to even severe adverse side effects, which have limited their clinical application. Cationic liposome as a novel non-viral carrier for co-delivery of gene and chemotherapy drugs in cancer gene therapy has already attracted more and more attention in recent years. Most importantly, this combined strategy can generate a significant synergistic effect, which can silence the related gene expression and increase the concentration of the intracellular chemotherapy drugs. This approach allows the use of a much lower dose of the chemotherapy drugs to achieve same therapeutic effect, which may have the potential for overcoming some major limitations of the conventional chemotherapy. In conclusion, co-delivery of gene and chemotherapy drugs with cationic liposome delivery system will play a vital role in the future and especially could be a promising clinical treatment for drug-resistant tumors.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Therapeutics / DNA / Drug Carriers / Genetic Therapy / Antineoplastic Combined Chemotherapy Protocols / Cations / Chemistry / Drug Delivery Systems / Gene Transfer Techniques / RNA, Small Interfering Limits: Animals / Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Therapeutics / DNA / Drug Carriers / Genetic Therapy / Antineoplastic Combined Chemotherapy Protocols / Cations / Chemistry / Drug Delivery Systems / Gene Transfer Techniques / RNA, Small Interfering Limits: Animals / Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2012 Type: Article