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Co-delivery of Adenovirus and Carmustine by Anionic Liposomes with Synergistic Anti-tumor Effects
- Source :
- Pharmaceutical Research. 29:145-157
- Publication Year :
- 2011
- Publisher :
- Springer Science and Business Media LLC, 2011.
-
Abstract
- To improve gene transducibility mediated by adenovirus (Ad) in cancer cells and further enhance anti-tumor effects by co-delivery.Calcium-induced phase change method was used to prepare the complex of anionic liposomes and adenovirus (AL/Ad5). Gene expression was qualitatively detected by X-gal staining and quantitatively detected by ELISA. Taking adenovirus-mediated stromal cell-derived factor-1α (Ad5-SDF1α) as therapeutic gene and carmustine (BCNU) as chemotherapeutic agent, a co-delivering system of AL/Ad5-SDF1α/BCNU was prepared and administered to tumor-bearing mice by intratumor injection.Enhanced LacZ gene transduction was obtained in B16 and Lewis lung carcinoma cells in vitro and in vivo. Complexes of AL/Ad5-SDF1α improved SDF1α gene expression and led to accumulation of dendritic cells among the murine B16 melanoma cells in vivo. This co-delivery system of AL/Ad5-SDF1α/BCNU could significantly suppress tumor growth and prolong survival of tumor-bearing mice.Through the co-delivering system, AL/Ad5-SDF1α could synergize with BCNU to improve the antitumor effect. It may be a promising strategy for solid tumor therapy.
- Subjects :
- Male
Indoles
Genetic Vectors
Pharmacology toxicology
Gene Expression
Pharmaceutical Science
Antineoplastic Agents
Injections, Intralesional
Adenoviridae
Mice
Transduction, Genetic
Tumor Cells, Cultured
Animals
Medicine
Pharmacology (medical)
Antineoplastic Agents, Alkylating
Pharmacology
Antitumor activity
Co delivery
Liposome
Carmustine
business.industry
Organic Chemistry
Drug Synergism
Galactosides
Genetic Therapy
Neoplasms, Experimental
Virology
Chemokine CXCL12
Mice, Inbred C57BL
Lac Operon
Liposomes
Cancer cell
Cancer research
Molecular Medicine
business
Biotechnology
medicine.drug
Subjects
Details
- ISSN :
- 1573904X and 07248741
- Volume :
- 29
- Database :
- OpenAIRE
- Journal :
- Pharmaceutical Research
- Accession number :
- edsair.doi.dedup.....cfee9eacc1680e4b7994b7f00867969b
- Full Text :
- https://doi.org/10.1007/s11095-011-0521-7