Polymeric micelles as potent islet amyloid inhibitors: Current advances and future perspectives

Jaskiran Kaur1, Monica Gulati2, Indu Pal Kaur3

  • 1School of Pharmaceutical Sciences, Lovely Professional University, Jalandhar-Delhi G.T. Road, Phagwara, Punjab 144411, India.

Drug Discovery Today
|March 29, 2023
PubMed

Insights

Polymeric micelles (PMs) offer a novel approach to treating diabetes mellitus (DM) by targeting misfolded islet amyloid polypeptide (IAPP) protein, a key factor in pancreatic beta cell damage. This review explores PM design for halting islet amyloidosis and discusses clinical translation challenges.

Area of Science:

  • Biomedical Engineering
  • Drug Delivery Systems
  • Endocrinology

Background:

  • Diabetes mellitus (DM) is a global health concern, often linked to pancreatic beta cell damage.
  • Current treatments fail to address the root cause of DM, such as islet amyloid polypeptide (IAPP) misfolding.
  • IAPP misfolding, implicated in over 90% of DM cases, stems from oxidative stress or genetic mutations.

Purpose of the Study:

  • To review advancements in designing polymeric micelles (PMs) for halting islet amyloidosis.
  • To elucidate the mechanisms and dynamics of PM-IAPP interactions.
  • To identify clinical challenges in translating PMs as anti-islet amyloidogenic therapies.

Main Methods:

  • Review of literature on polymeric micelle design for amyloidosis.
  • Analysis of studies on PM-IAPP interaction mechanisms.
  • Discussion of clinical trial data and regulatory hurdles for PM-based DM therapies.

Main Results:

  • Polymeric micelles demonstrate potential in targeting and preventing IAPP misfolding.
  • Understanding PM-IAPP dynamics is crucial for therapeutic efficacy.
  • Significant clinical and regulatory challenges impede the translation of PMs into clinical practice.

Conclusions:

  • Polymeric micelles represent a promising therapeutic strategy for diabetes by targeting islet amyloidosis.
  • Further research into PM-IAPP interactions and robust clinical trials are necessary.
  • Overcoming translational challenges is key to realizing the potential of PMs for diabetes treatment.

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