Milk derived colloid as a novel drug delivery carrier for breast cancer

Masamichi Hayashi1, Nissim Silanikove, Xiaofei Chang

  • 1a Department of Otolaryngology-Head and Neck Surgery ; Johns Hopkins School of Medicine ; Baltimore , MD USA.

Insights

Researchers developed a novel nanoparticle, MDC, from milk-derived colloid to deliver chemotherapy drugs. MDC-conjugated doxorubicin (MDC-Dox) effectively inhibited triple-negative breast cancer growth in preclinical models, offering a promising strategy against drug resistance.

Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Oncology

Background:

  • Triple-negative breast cancer (TNBC) presents a poor prognosis, particularly when chemotherapy resistance develops.
  • Nanoparticle-based drug delivery systems show promise in overcoming chemotherapy resistance.
  • A novel nanoparticle component, MDC, was synthesized from milk-derived colloid.

Purpose of the Study:

  • To evaluate the anti-cancer effects of the novel milk-derived colloid nanoparticle (MDC).
  • To assess the efficacy of doxorubicin conjugated to MDC (MDC-Dox) against cancer cell lines and in vivo tumor models.

Main Methods:

  • In vitro experiments were conducted on cancer cell lines, including those with high EGFR expression.
  • In vivo studies involved a mouse melanoma model and a primary tumor-derived breast xenograft model.
  • MDC-Dox efficacy was compared against MDC alone and free doxorubicin (Dox).

Main Results:

  • MDC-Dox demonstrated superior cancer cell growth inhibition compared to MDC alone, especially in EGFR-high expressing cell lines.
  • MDC-Dox significantly suppressed tumor growth in a mouse melanoma model versus free Dox.
  • In a breast xenograft model, MDC-Dox induced partial tumor regression in one mouse, while free Dox showed no tumor suppression.

Conclusions:

  • The novel milk-derived colloid nanoparticle (MDC) can be conjugated with drugs and acts as a tumor-specific carrier.
  • MDC-Dox exhibits significant anti-cancer activity, suggesting potential for overcoming drug resistance in TNBC.
  • Further research is warranted to explore MDC's safety and efficacy with various anti-cancer drugs in diverse drug-resistant breast cancer models.

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