Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Glucagon-like Receptor Agonists01:24

Glucagon-like Receptor Agonists

854
Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
854
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors01:19

Oral Hypoglycemic Agents: α-Glucosidase Inhibitors

526
α-glucosidase inhibitors, including acarbose (Precose), miglitol (Glyset), and voglibose (Voglib) (primarily available in Asia), are drugs that control blood sugar levels by delaying the digestion of starch and disaccharides. They achieve this by inhibiting α-glucosidase enzymes in the intestine, which slow the absorption of carbohydrates in the intestine, which in turn leads to a prolonged release of the glucoregulatory hormone GLP-1 from intestinal L-cells.
Acarbose and miglitol are...
526
Dipeptidyl Peptidase 4 Inhibitors01:23

Dipeptidyl Peptidase 4 Inhibitors

598
Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
598
Insulin: Biosynthesis, Chemistry, and Preparation01:25

Insulin: Biosynthesis, Chemistry, and Preparation

1.2K
The endoplasmic reticulum (ER) of pancreatic β-cells synthesizes preproinsulin, which consists of a signal peptide, A and B chains, and a C-peptide. Preproinsulin is then cleaved and folded into proinsulin, which translocates to the Golgi apparatus for sorting and packaging into secretory granules. In these granules, enzymatic clipping generates insulin and C-peptide.
Damage or functional impairment of β-cells inhibits insulin production, leading to diabetes. Diabetes treatment...
1.2K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Biotherapeutic strategies for quorum quenching in Salmonella Typhi: a review.

Archives of microbiology·2026
Same author

Molecular docking: a computational approach for the discovery of novel targets against visceral leishmaniasis.

Journal of molecular modeling·2026
Same author

Deciphering the bioactive properties of sodium lignosulfonate (LIG) and LIG-induced cell death of human fungal pathogen <i>Candida albicans</i>.

In silico pharmacology·2025
Same author

Computational evidence of cancer and reproductive toxicological potential from short-chain PFAS exposure through network toxicology and docking approaches.

Toxicology mechanisms and methods·2025
Same author

Role of the microbiome in diabetic wound healing: implications for new therapeutic approaches.

Archives of microbiology·2025
Same author

Upcoming generation nanoengineered antimicrobial delivery system for targeting multidrug-resistant microbes.

Critical reviews in biotechnology·2025

Related Experiment Video

Updated: Jan 18, 2026

Sustained Administration of &#946;-cell Mitogens to Intact Mouse Islets Ex Vivo Using Biodegradable Poly(lactic-co-glycolic acid) Microspheres
09:31

Sustained Administration of β-cell Mitogens to Intact Mouse Islets Ex Vivo Using Biodegradable Poly(lactic-co-glycolic acid) Microspheres

Published on: November 5, 2016

7.7K

Exploring multi-functional biopolymer polyhydroxyalkanoates in diabetes treatment.

Gunjan Adwani1, Sharda Bharti1, Awanish Kumar1

  • 1Department of Biotechnology, National Institute of Technology, Raipur, Chhattisgarh, India.

Journal of Biomaterials Science. Polymer Edition
|May 29, 2025
PubMed
Summary

Polyhydroxyalkanoates (PHAs) show promise as biomaterials for diabetes management, offering controlled drug delivery and wound healing. Further research is needed to overcome production challenges and fully realize their therapeutic potential.

Keywords:
Poly(3-hydroxybutyrate)diabetesinsulin deliverypoly(4-hydroxybutyrate)wound healing

More Related Videos

The Synthesis of RGD-functionalized Hydrogels as a Tool for Therapeutic Applications
09:30

The Synthesis of RGD-functionalized Hydrogels as a Tool for Therapeutic Applications

Published on: October 7, 2016

11.9K
Tracking Hypoxic Signaling within Encapsulated Cell Aggregates
09:14

Tracking Hypoxic Signaling within Encapsulated Cell Aggregates

Published on: December 16, 2011

11.0K

Related Experiment Videos

Last Updated: Jan 18, 2026

Sustained Administration of &#946;-cell Mitogens to Intact Mouse Islets Ex Vivo Using Biodegradable Poly(lactic-co-glycolic acid) Microspheres
09:31

Sustained Administration of β-cell Mitogens to Intact Mouse Islets Ex Vivo Using Biodegradable Poly(lactic-co-glycolic acid) Microspheres

Published on: November 5, 2016

7.7K
The Synthesis of RGD-functionalized Hydrogels as a Tool for Therapeutic Applications
09:30

The Synthesis of RGD-functionalized Hydrogels as a Tool for Therapeutic Applications

Published on: October 7, 2016

11.9K
Tracking Hypoxic Signaling within Encapsulated Cell Aggregates
09:14

Tracking Hypoxic Signaling within Encapsulated Cell Aggregates

Published on: December 16, 2011

11.0K

Area of Science:

  • Biomaterials Science
  • Polymer Chemistry
  • Endocrinology

Background:

  • Diabetes mellitus is a global chronic metabolic disorder characterized by hyperglycemia.
  • Current treatments for diabetes require non-invasive insulin delivery and effective wound healing therapeutics.
  • There is a significant need for novel biomaterials to enhance diabetes management.

Purpose of the Study:

  • To review the therapeutic potential of Polyhydroxyalkanoates (PHAs) in diabetes management.
  • To explore the application of PHAs as advanced biomaterials for antidiabetic and wound healing therapies.
  • To highlight the challenges and future directions for PHA utilization in diabetes care.

Main Methods:

  • Literature review focusing on Polyhydroxyalkanoates (PHAs) in biomedical applications.
  • Analysis of PHA properties including biocompatibility, biodegradability, and controlled drug release.
  • Examination of PHA applications in bioartificial pancreas development and wound healing.

Main Results:

  • PHAs exhibit biocompatibility, biodegradability, and can be synthesized into scaffolds and nanomaterials for sustained drug delivery.
  • PHAs demonstrate antidiabetic and antimicrobial activities, beneficial for wound healing.
  • PHA-based scaffolds provide a supportive environment for pancreatic cell encapsulation in bioartificial pancreas designs.

Conclusions:

  • PHAs offer a versatile platform for developing advanced diabetes therapeutics, including controlled insulin delivery and improved wound healing.
  • Challenges such as high production costs and market integration require further investigation.
  • Continued research is essential to fully harness the therapeutic capabilities of PHAs for comprehensive diabetes management.