4.5 Article

The Controlled Release and Anti-Inflammatory Activity of a Tetramethylpyrazine-Loaded Thermosensitive Poloxamer Hydrogel

期刊

PHARMACEUTICAL RESEARCH
卷 36, 期 4, 页码 -

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11095-019-2580-0

关键词

anti-inflammatory test; controlled release; gelling temperature; tetramethylpyrazine; thermosensitive poloxamer hydrogel

资金

  1. Natural Science Foundation of Anhui Province of China [1608085MH227]
  2. 2017 Anhui University of Chinese Medicine annual innovation training program for College Students [2017171, 2017142]
  3. Natural Science Fund of Anhui University of Chinese Medicine [2010zr004A]
  4. Kangyuan Fund [KYCX201001]
  5. Anhui province science and technology special fund project [13Z04013]
  6. Natural Science Foundation [61573615]

向作者/读者索取更多资源

PurposeTetramethylpyrazine-loaded poloxamer hydrogel materials were studied to achieve the controlled release of tetramethylpyrazine.MethodsFirst, hydrogels having different concentrations of poloxamer 407 and poloxamer 188 were prepared. The gelling temperature and viscosity were measured. Second, we investigated the tetramethylpyrazine release rate from the thermosensitive poloxamer hydrogel materials in vitro and ex vivo. Finally, further study of the pharmacological efficacy of the tetramethylpyrazine-loaded thermosensitive poloxamer hydrogel materials was also investigated in vivo.ResultsThe in vitro, ex vivo and in vivo experimental results showed that the tetramethylpyrazine-loaded poloxamer hydrogel with the appropriate gelling temperature, good adhesion and easy preparation controlled the release of tetramethylpyrazine.ConclusionsThe hydrogel with the suitable nasal temperature and a satisfactory adhesion was selected. The relevant tests were carried out, including the determination of the concentration of drugs in the brain homogenate and the anti-inflammatory test after different modes of administration. So the poloxamer hydrogel was a novel carrier to deliver TMP to pass across the blood brain barrier via nasal administration.

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