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1.
Langmuir ; 27(10): 5874-8, 2011 May 17.
Artigo em Inglês | MEDLINE | ID: mdl-21488607

RESUMO

We have developed a potential radiation-sensitive drug-delivery system using active diselenide-containing block co-polymer aggregates in aqueous solution that can load and release anticancer drugs. These aggregates were sensitive to even a low dose of γ-radiation, such as 5 Gy, which is close to the radiation dose received by patients during a single radiotherapy treatment. This line of research may open an avenue for the combination of radiotherapy and chemotherapy.


Assuntos
Portadores de Fármacos/química , Micelas , Polímeros/química , Compostos de Selênio/química , Antineoplásicos/uso terapêutico , Terapia Combinada , Portadores de Fármacos/toxicidade , Raios gama , Células Hep G2 , Humanos , Neoplasias/tratamento farmacológico , Neoplasias/radioterapia , Polietilenoglicóis/química , Compostos de Selênio/toxicidade , Água/química
2.
Chem Pharm Bull (Tokyo) ; 59(5): 559-63, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21532192

RESUMO

A novel block ionomer complex micelles as drug carrier is developed utilizing self-assemble of poly(ethylene glycol)-block-poly(acrylic acid) (PEG-b-PAA) and cadmium chloride. This micelles are characterized to be have good bio-compatibility, hydrophilicity, passive targeting and sustained slow release property which shows great potential for liver cancer therapy. Block ionomer complex micelles based on PEG-b-PAA and cadmium chloride can self-assemble in distilled water, and Cd(²+) agent is entrapped into the core stabilized by PEG shells. Results showed the block ionomer complex micelles to be spherically shaped. Cadmium was incorporated easily into the ionic core with remarkably high efficiency (34.25% weight (wt)/wt). The cadmium-loaded polymeric micelles exhibited sustained and slow release behavior of cadmium and a potent cytotoxicity against SMMC-7721 in vitro. This novel block ionomer complex micelles with cores of metal antitumor drug indicates to be potential carriers for effective drug delivery.


Assuntos
Acrilatos/farmacologia , Antineoplásicos/farmacologia , Cloreto de Cádmio/farmacologia , Sistemas de Liberação de Medicamentos/métodos , Polietilenoglicóis/farmacologia , Acrilatos/administração & dosagem , Acrilatos/química , Antineoplásicos/administração & dosagem , Antineoplásicos/química , Cloreto de Cádmio/administração & dosagem , Cloreto de Cádmio/química , Carcinoma Hepatocelular/metabolismo , Carcinoma Hepatocelular/patologia , Humanos , Neoplasias Hepáticas/metabolismo , Neoplasias Hepáticas/patologia , Micelas , Polietilenoglicóis/administração & dosagem , Polietilenoglicóis/química , Células Tumorais Cultivadas
3.
Zhongguo Gu Shang ; 33(12): 1175-8, 2020 Dec 25.
Artigo em Zh | MEDLINE | ID: mdl-33369328

RESUMO

Titanium alloy has good biological properties and is commonly used in orthopedics, but its bone integrity and antibacterial properties are poor, so surface modification is needed to make up for its shortcomings. Chitosan has good biocompatibility and film forming ability, and can be used as a carrier to introduce the target drug to the surface of titanium alloy, which can effectively improve the biological properties of titanium alloy materials and increase its application range. In this paper, the related research of chitosan surface modified titanium alloy materials in recent years is summarized. The modification methods of chitosan coating, the improvement of osteogenesisand antibacterial properties of titanium alloy materials are discussed in order to provide guidance for the clinical application of coating modification of titanium alloy materials.


Assuntos
Quitosana , Ortopedia , Ligas , Antibacterianos/farmacologia , Propriedades de Superfície , Titânio
4.
Artigo em Zh | MEDLINE | ID: mdl-24844025

RESUMO

OBJECTIVE: To investigate the feasibility of tissue engineered periosteum (TEP) constructed by porcine small intestinal submucosa (SIS) and bone marrow mesenchymal stem cells (BMSCs) of rabbit to repair the large irregular bone defects in allogenic rabbits. METHODS: The BMSCs were cultivated from the bone marrow of New Zealand white rabbits (aged, 2 weeks-1 month). SIS was fabricated by porcine proximal jejunum. The TEP constructed by SIS scaffold and BMSCs was prepared in vitro. Eighteen 6-month-old New Zealand white rabbits whose scapula was incompletely resected to establish one side large irregular bone defects (3 cm x 3 cm) model. The bone defects were repaired with TEP (experimental group, n = 9) and SIS (control group, n = 9), respectively. At 8 weeks after operation, the rabbits were sacrificed, and the implants were harvested. The general condition of the rabbits was observed; X-ray radiography and score according to Lane-Sandhu criteria, and histological examination (HE staining and Masson staining) were performed. RESULTS: After operation, all animals had normal behavior and diet; the incision healed normally. The X-ray results showed new bone formation with normal bone density in the defect area of experimental group; but no bone formation was observed in control group. The X-ray score was 6.67 +/- 0.32 in experimental group and was 0.32 +/- 0.04 in control group, showing significant difference (t = 19.871, P = 0.001). The general observation of the specimens showed bone healing at both ends of the defect, and the defect was filled by new bone in experimental group; no new bone formed in the control group. The histological staining showed new bone tissue where there were a lot of new vessels and medullary cavity, and no macrophages or lymphocytes infiltration was observed in the defect area of experimental group; only some connective tissue was found in the control group. CONCLUSION: TEP constructed by porcine SIS and BMSCs of rabbit can form new bone in allogenic rabbit and has the feasibility to repair the large irregular bone defects.


Assuntos
Mucosa Intestinal , Células-Tronco Mesenquimais/citologia , Osteogênese , Periósteo/transplante , Escápula/cirurgia , Engenharia Tecidual/métodos , Animais , Células da Medula Óssea/citologia , Substitutos Ósseos , Células Cultivadas , Modelos Animais de Doenças , Implantes Experimentais , Intestino Delgado , Masculino , Coelhos , Distribuição Aleatória , Escápula/patologia , Suínos , Alicerces Teciduais , Transplante Homólogo
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