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Antitumoral effect and reduced systemic toxicity in mice after intra-tumoral injection of an in vivo solidifying calcium sulfate formulation with docetaxel

Grudén, Stefan (författare)
LIDDS AB, Uppsala, Sweden
Sandelin, Martin, 1976- (författare)
Uppsala universitet,Lungmedicin och allergologi
Rasanen, Veera (författare)
Uppsala universitet,Institutionen för immunologi, genetik och patologi
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Micke, Patrick (författare)
Uppsala universitet,Institutionen för immunologi, genetik och patologi
Hedeland, Mikael (författare)
Uppsala universitet,Avdelningen för analytisk farmaceutisk kemi,National Veterinary Institute (SVA), Department of Chemistry, Environment and Feed Hygiene, Uppsala, Sweden
Axén, Niklas (författare)
LIDDS AB, Uppsala, Sweden
Jeansson, Marie (författare)
Uppsala universitet,Vaskulärbiologi,Jeansson
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 (creator_code:org_t)
Elsevier BV, 2017
2017
Engelska.
Ingår i: European journal of pharmaceutics and biopharmaceutics. - : Elsevier BV. - 0939-6411 .- 1873-3441. ; 114, s. 186-193
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • BackgroundDocetaxel is a cytostatic agent approved for treatment of non-small cell lung cancer as well as other cancers. Although docetaxel is an effective cytostatic agent, its effectiveness in clinical practice is associated with a variety of acute and long term side-effects. To overcome systemic side-effects, a slow release formulation based on calcium sulfate with docetaxel for intra-tumoral administration was developed.MethodsTwo formulations with the calcium sulfate NanoZolid technology were generated with a twofold difference in docetaxel drug load. The formulations were injected intra-tumorally as a paste which solidified within the tumor. The effects of the two intra-tumoral injection formulations were tested in female mice (n = 60) inoculated with subcutaneous Lewis lung carcinoma cells. The two formulations were compared to systemic intraperitoneal injection of docetaxel and a placebo formulation without docetaxel. Tumor volumes were measured and systemic side-effects were evaluated using body weight and cell counts from whole blood as well as plasma concentrations.ResultsBoth docetaxel formulations showed a significantly higher antitumor efficacy compared to placebo, which was comparable to that of systemic administration of docetaxel. Moreover, the intra-tumoral formulations with docetaxel showed reduced systemic toxicity compared to systemic treatment, including less weight loss and no decrease in blood cell counts.ConclusionsThe results suggest that intra-tumoral slow release calcium sulfate based formulations with docetaxel can be an alternative strategy as an efficient local antitumoral treatment with reduced systemic toxicity.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Bioresorbable
Calcium sulfate
Docetaxel
Intratumoral
Lewis lung carcinoma
Non-small cell lung cancer
Slow release formulation
Medicinsk vetenskap
Medical Science

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