AI Article Synopsis

  • Recent research highlights the potential anti-tumor effects of cannabis extracts, particularly THC and CBD, in treating glioblastoma using a specially designed nanoemulsion (NE).
  • In tests with rats, the new nanoemulsion (NED) showed better drug delivery, increased hemocompatibility, and significantly reduced tumor size compared to bulk drugs and a carrier without the active components.
  • NED treatment resulted in a notable survival increase (up to 51 days) and demonstrated effectiveness without major side effects, suggesting its promise for treating brain glioblastoma.

Article Abstract

Recently, the anti-tumor effects of cannabis extract on various cancers have attracted the attention of researchers. Here, we report a nanoemulsion (NE) composition designed to enhance the delivery of two active components in cannabis extracts (∆9-Tetrahydrocannabinol (THC) and Cannabidiol (CBD)) in an animal model of glioblastoma. The efficacy of the NE containing the two drugs (NED) was compared with the bulk drugs and carrier (NE without the drugs) using the C6 tumor model in rats. Hemocompatibility factors (RBC, MCV, MCH, MCHC, RDW, PPP, PT and PTT) were studied to determine the potential in vivo toxicity of NED. The optimized NED with mean ± SD diameter 29 ± 6 nm was obtained. It was shown that by administering the drugs in the form of NED, the hemocompatibility increased. Cytotoxicity studies indicated that the NE without the active components (i.e. mixture of surfactants and oil) was the most cytotoxic group, while the bulk group had no toxicity. From the in vivo MRI and survival studies, the NED group had maximum efficacy (with ~4 times smaller tumor volume on day 7 of treatment, compared with the control. Also, survival time of the control, bulk drug, NE and NED were 9, 4, 12.5 and 51 days, respectively) with no important adverse effects. In conclusion, the NE containing cannabis extract could be introduced as an effective treatment in reducing brain glioblastoma tumor progression.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11460059PMC
http://dx.doi.org/10.1186/s40360-024-00788-wDOI Listing

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