BioPerine Encapsulated Nanoformulation for Overcoming Drug-Resistant Breast Cancers

Sindhu C Pillai1, Ankita Borah1, Amandeep Jindal2

  • 1Bio-Nano Electronics Research Centre, Graduate School of Interdisciplinary New Science, Toyo University, Saitama 350-8585, Japan.

Insights

This study introduces a novel nanoparticle system using BioPerine from black pepper to overcome breast cancer drug resistance. The nanoparticles effectively suppressed P-glycoprotein (P-gp) expression, enhancing chemotherapy

Area of Science:

  • Nanomedicine
  • Cancer Biology
  • Pharmacology

Background:

  • Tumor heterogeneity and P-glycoprotein (P-gp) overexpression drive multidrug resistance (MDR) in breast cancer, limiting therapeutic efficacy.
  • Traditional chemotherapy faces significant challenges against drug-resistant breast cancer cell lines like MDA-MB 453.
  • Phytonutrients, specifically alkaloids, show promise in inhibiting P-gp and overcoming MDR.

Purpose of the Study:

  • To develop and evaluate a novel nano-drug delivery system for BioPerine, a black pepper alkaloid derivative.
  • To assess the efficacy of BioPerine-loaded chitosan-polyethylene glycol coated polylactic acid (CS-PEG-BioPerine-PLA) nanoparticles in suppressing P-gp expression in breast cancer cells.
  • To improve the bioavailability and therapeutic potential of BioPerine against drug-resistant breast cancer.

Main Methods:

  • Fabrication of CS-PEG-BioPerine-PLA hybrid polymeric nanoparticles.
  • Characterization of nanoparticle morphology, size, and drug release kinetics.
  • In vitro evaluation of cytotoxicity and P-gp expression downregulation in MDA-MB 453 cells.
  • Comparison with the commercial P-gp inhibitor, verapamil hydrochloride.

Main Results:

  • CS-PEG-BioPerine-PLA nanoparticles exhibited spherical morphology (316 nm) with enhanced aqueous solubility and sustained drug release.
  • Nanoparticles significantly increased in vitro cytotoxicity in MDA-MB 453 cells.
  • Demonstrated effective downregulation of P-gp expression, outperforming verapamil hydrochloride.

Conclusions:

  • The developed CS-PEG-BioPerine-PLA nanoparticle system offers a promising approach to enhance BioPerine's bioavailability and efficacy.
  • This nano-drug delivery system shows potential in overcoming P-gp-mediated multidrug resistance in breast cancer.
  • BioPerine-based nanoparticles represent a viable strategy for combination therapy to combat drug-resistant cancers.

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