[Interaction between insulin with liposome]

Xuan Zhang1, Xian-rong Qi, Qiang Zhang

  • 1School of Pharmaceutical Science, Peking University, Beijing 100083, China.

Insights

This study investigated insulin and liposome interactions using spectroscopy and calorimetry. Results reveal a weak interaction between insulin and liposomes, with only 0.2% combination observed.

Area of Science:

  • Biochemistry
  • Physical Chemistry
  • Drug Delivery Systems

Context:

  • Liposomes are widely used as drug delivery vehicles.
  • Understanding drug-carrier interactions is crucial for optimizing delivery efficacy.
  • Insulin delivery faces challenges due to its nature and potential interactions with carriers.

Purpose:

  • To characterize the interaction between insulin and liposomes.
  • To quantify the binding affinity and nature of insulin-liposome association.
  • To evaluate the stability of insulin within liposomal formulations.

Summary:

  • Insulin-liposome interactions were assessed using fluorescence spectroscopy and microcalorimetry.
  • Fluorescence quenching studies and thermodynamic analysis indicated weak binding.
  • High-performance liquid chromatography (HPLC) confirmed minimal insulin association with liposomes (0.2% combination).

Impact:

  • The findings suggest limited direct interaction between insulin and liposomes.
  • This information is vital for designing effective insulin-loaded liposomal formulations.
  • Further research may explore modifications to enhance insulin encapsulation and stability in liposomes.
Abstract

Related Concept Videos

Insulin Secretory Vesicles01:05

Insulin Secretory Vesicles

Insulin secretory vesicles release insulin to stimulate blood glucose uptake and regulate carbohydrate metabolism. When the blood glucose levels increase, glucose enters the pancreatic β-islet cells through glucose transporters. Once inside, glucose is metabolized through glycolysis, the citric acid cycle, and the electron transport chain, producing ATP. This increase in ATP concentration closes ATP-sensitive potassium channels, leading to depolarization of the membrane and the opening of...
Insulin: The Receptor and Signaling Pathways01:28

Insulin: The Receptor and Signaling Pathways

Insulin action is mediated through a receptor tyrosine kinase, akin to the IGF-1 receptor. The number of receptors per cell varies significantly, from 40 on erythrocytes to 300,000 on adipocytes and hepatocytes. The insulin receptor consists of linked α/β subunit dimers, forming a heterotetramer glycoprotein with two extracellular α subunits and two β subunits spanning the membrane. The α subunits inhibit the inherent tyrosine kinase activity of the β subunits, but this inhibition is released...
Insulin: Biosynthesis, Chemistry, and Preparation01:25

Insulin: Biosynthesis, Chemistry, and Preparation

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 primarily uses...
Insulin Formulations: Types and Delivery01:27

Insulin Formulations: Types and Delivery

Insulin preparations are categorized by their duration of action into short-acting and long-acting types. Two strategies are used to modify insulin's absorption and pharmacokinetic profile: slowing the absorption post-subcutaneous injection, or altering human insulin's amino acid sequence or protein structure. These changes retain the insulin's ability to bind to the insulin receptor, but alter its behavior in solution or after injection.
Short-acting insulins are divided into rapid-acting...
Receptor-mediated Endocytosis01:48

Receptor-mediated Endocytosis

Receptor-mediated endocytosis is a process through which bulk amounts of specific molecules can be imported into a cell after binding to cell surface receptors. The molecules bound to these receptors are taken into the cell through inward folding of the cell surface membrane, which is eventually pinched off into a vesicle within the cell. Structural proteins, such as clathrin, coat the budding vesicle and give it its round form.Clathrin-Mediated Endocytosis of LDLOne well-characterized example...
Insulin: Dosing Regimen and Adverse Effects01:16

Insulin: Dosing Regimen and Adverse Effects

Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...