MedPath

Dextran

Generic Name
Dextran
Brand Names
Bion Tears, Colirio Ocusan, Genteal Tears, Genteal Tears Mild, Tears Naturale, Tears Renewed
Drug Type
Small Molecule
CAS Number
9004-54-0

Overview

Dextran is a polysaccharide that differs from others in that its glucose units are joined together 1:6 glucoside links. The main chain of glucose has short branches at frequent intervals which are probably joined by 1:3 and 1:4 glucoside links. The chains can be composed of about 200,000 glucose units. Many bacteria, like Leuconostoc, can synthesize dextran from sucrose, and this activity is used commercially to obtain dextran. Dextran 40 is a sterile, nonpyrogenic preparation of low molecular weight dextran (average mol. wt. 40,000) in 5% Dextrose Injection or 0.9% Sodium Chloride Injection. It is administered by intravenous infusion. Dextran 75 is a complex branched glucan with an average molecular weight 75000 Daltons. It is produced from certain bacteria that with α-1,6 glycosidic linkages between glucose molecules and α-1,3 linkages between branches. When labelled with technetium Tc99m, dextran 75 is intravenously administered as an imaging agent to detect and diagnose conditions in the vascular compartment such as pericardial effusion or ventricular aneurysm.

Indication

Dextran is used as the restoration of blood mass during surgical interventions if there is hypovolemia due to trauma or dehydration. It is as well used after the presence of hemorrhage in cases of blood loss to a level inferior to 15% of the blood mass, if compatibility test cannot be completed or when blood lots need to be tested for pathogen detection. Dextran is also used for the prevention of profound postoperative venous thrombosis. Dextran as well presents ophthalmic applications as solutions or ointments for the temporary relief of xerophthalmia or minor ocular irritations.

Associated Conditions

  • Blood Circulation Disorder
  • Capillary disorder
  • Dry Eyes
  • Ocular Irritation
  • Pulmonary Embolism
  • Pulmonary Embolism caused by procedures associated with a high incidence of thromboembolic complications
  • Shock
  • Thrombosis
  • Venous Thrombosis (Disorder)
  • Venous Thrombosis caused by procedures associated with a high incidence of thromboembolic complications

Research Report

Published: Sep 24, 2025

Dextran (DB09255): A Comprehensive Pharmacological and Clinical Monograph

Executive Summary

Dextran is a complex, variable molecular weight polysaccharide of microbial origin, characterized by a dual pharmacological profile as both a plasma volume expander and an antithrombotic agent. Its primary structure, consisting of an α-1,6 linked D-glucose backbone with periodic branches, dictates its physicochemical properties and, consequently, its therapeutic applications and risks. The clinical utility of Dextran is fundamentally governed by its molecular weight, with two principal fractions, Dextran 40 and Dextran 70, exhibiting distinct pharmacokinetic and pharmacodynamic profiles.

As a plasma volume expander, Dextran exerts a colloid osmotic pressure within the intravascular space, drawing fluid from the interstitium to restore circulating volume. This hemodynamic effect is central to its indication for the adjunctive treatment of hypovolemic shock arising from hemorrhage, surgery, or trauma. Concurrently, Dextran modulates hemostasis by reducing erythrocyte aggregation, decreasing platelet adhesiveness, lowering levels of key coagulation factors, and promoting fibrinolysis. These antithrombotic properties underpin its use in the prophylaxis of venous thromboembolism during high-risk surgical procedures.

Beyond these primary roles, Dextran serves as a critical carrier molecule in the Iron Dextran complex, a parenteral formulation for treating iron-deficiency anemia in patients who cannot tolerate or respond to oral iron. In this capacity, the Dextran shell stabilizes the ferric hydroxide core, enabling a controlled release of iron and mitigating toxicity. Dextran is also a ubiquitous component in ophthalmic lubricating solutions and has emerged as a versatile platform technology in biomedical research and advanced drug delivery systems, including nanoparticles, hydrogels, and chromatography matrices.

Continue reading the full research report

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2022/09/07
N/A
ENROLLING_BY_INVITATION
2022/04/06
Phase 4
Completed
Andover Research Eye Institute
2022/03/04
Phase 4
Completed
Andover Research Eye Institute
2021/08/17
N/A
Recruiting
2018/02/15
Not Applicable
UNKNOWN
LanZhou University
2017/07/07
Not Applicable
Completed
Huaxia Eye Hospital Group
2017/03/03
Phase 2
Completed
2017/02/23
Not Applicable
UNKNOWN
Tung Wah Hospital
2016/12/14
Not Applicable
UNKNOWN
Sun Yat-sen University
2016/08/11
Phase 1
Completed
Joseph B. Ciolino, MD

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Hospira, Inc.
0409-7419
INTRAVENOUS
10 g in 100 mL
2/15/2023
Hospira, Inc.
0409-7418
INTRAVENOUS
10 g in 100 mL
2/15/2023
DLC Laboratories, Inc.
24286-1575
OPHTHALMIC
1 mg in 1 mL
4/18/2025
Preferred PHarmaceuticals Inc.
68788-8635
OPHTHALMIC
0.1 g in 100 mL
5/7/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
DACROLUX 3MG/ML +1MG/ML COLIRIO EN SOLUCIÓN
Reva Health Europe S.L.
58742
COLIRIO EN SOLUCIÓN
Sin Receta
Not Commercialized
RHEOMACRODEX 10% SALINO
Fresenius Kabi España, S.A.U.
39627
SOLUCIÓN PARA PERFUSIÓN
Uso Hospitalario
Not Commercialized

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.