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1.
Drug Deliv ; 23(1): 167-73, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-24786643

RESUMO

CONTEXT: Inadequate penetration of the blood-brain barrier (BBB) by systemically administered chemotherapies including carboplatin is implicated in their failure to improve prognosis for patients with glioblastoma. Convection-enhanced delivery (CED) of carboplatin has the potential to improve outcomes by facilitating bypass of the BBB. OBJECTIVE: We report the first use of an implantable CED system incorporating a novel transcutaneous bone-anchored port (TBAP) for intermittent CED of carboplatin in a patient with recurrent glioblastoma. MATERIALS AND METHODS: The CED catheter system was implanted using a robot-assisted surgical method. Catheter targeting accuracy was verified by performing intra-operative O-arm imaging. The TBAP was implanted using a skin-flap dermatome technique modeled on bone-anchored hearing aid surgery. Repeated infusions were performed by attaching a needle administration set to the TBAP. Drug distribution was monitored with serial real-time T2-weighted magnetic resonance imaging (MRI). RESULTS: All catheters were implanted to within 1.5 mm of their planned target. Intermittent infusions of carboplatin were performed on three consecutive days and repeated after one month without the need for further surgical intervention. Infused volumes of 27.9 ml per day were well tolerated, with the exception of a single seizure episode. Follow-up MRI at eight weeks demonstrated a significant reduction in the volume of tumor enhancement from 42.6 ml to 24.6 ml, and was associated with stability of the patient's clinical condition. CONCLUSION: Reduction in the volume of tumor enhancement indicates that intermittent CED of carboplatin has the potential to improve outcomes in glioblastoma. The novel technology described in this report make intermittent CED infusion regimes an achievable treatment strategy.


Assuntos
Antineoplásicos/administração & dosagem , Antineoplásicos/uso terapêutico , Neoplasias Encefálicas/tratamento farmacológico , Carboplatina/administração & dosagem , Carboplatina/uso terapêutico , Sistemas de Liberação de Medicamentos/métodos , Glioblastoma/tratamento farmacológico , Administração Cutânea , Antineoplásicos/efeitos adversos , Carboplatina/efeitos adversos , Cateteres de Demora , Convecção , Epilepsia Generalizada/complicações , Feminino , Humanos , Infusões Intravenosas , Imageamento por Ressonância Magnética , Pessoa de Meia-Idade , Robótica
2.
PLoS One ; 10(7): e0132266, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26186224

RESUMO

We currently use Convection-Enhanced Delivery (CED) of the platinum-based drug, carboplatin as a novel treatment strategy for high grade glioblastoma in adults and children. Although initial results show promise, carboplatin is not specifically toxic to tumour cells and has been associated with neurotoxicity at high infused concentrations in pre-clinical studies. Our treatment strategy requires intermittent infusions due to rapid clearance of carboplatin from the brain. In this study, carboplatin was encapsulated in lactic acid-glycolic acid copolymer (PLGA) to develop a novel drug delivery system. Neuronal and tumour cytotoxicity were assessed in primary neuronal and glioblastoma cell cultures. Distribution, tissue clearance and toxicity of carboplatin nanoparticles following CED was assessed in rat and porcine models. Carboplatin nanoparticles conferred greater tumour cytotoxicity, reduced neuronal toxicity and prolonged tissue half-life. In conclusion, this drug delivery system has the potential to improve the prognosis for patients with glioblastomas.


Assuntos
Carboplatina/uso terapêutico , Convecção , Sistemas de Liberação de Medicamentos , Glioblastoma/tratamento farmacológico , Ácido Láctico/química , Nanopartículas/química , Ácido Poliglicólico/química , Animais , Morte Celular/efeitos dos fármacos , Linhagem Celular Tumoral , Células Cultivadas , Endocitose/efeitos dos fármacos , Glioblastoma/patologia , Hipocampo/patologia , Humanos , Masculino , Nanopartículas/toxicidade , Neurotoxinas/toxicidade , Copolímero de Ácido Poliláctico e Ácido Poliglicólico , Ratos Wistar , Sus scrofa
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