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Updated: May 5, 2026

Rapid Point-of-Care Assay of Enoxaparin Anticoagulant Efficacy in Whole Blood
Published on: October 12, 2012
Novel experimental and clinical therapeutic uses of low-molecular-weight heparin/protamine microparticles
Satoko Kishimoto1, Masayuki Ishihara, Megumi Takikawa
1Research Institute, National Defense Medical College, 3-2 Namiki, Tokorozawa, Saitama 359-8513, Japan. ishihara@ndmc.ac.jp.
Abstract:
Low-molecular-weight heparin/protamine microparticles (LMW-H/P MPs) were produced as a carrier for heparin-binding growth factors (GFs) and for various adhesive cells. A mixture of low-molecular-weight heparin (MW: approximately 5000 Da, 6.4 mg/mL) and protamine (MW: approximately 3000 Da, 10 mg/mL) at a ratio of 7:3 (vol:vol) yields a dispersion of microparticles (0.5-3 µm in diameter). LMW-H/P MPs immobilize, control the release and protect the activity of GFs. LMW-H/P MPs can also bind to cell surfaces, causing these cells to interact with the LMW-H/P MPs, inducing cells/MPs-aggregate formation and substantially promoting cellular viability. Furthermore, LMW-H/P MPs can efficiently bind to tissue culture plates and retain the binding of important GFs, such as fibroblast growth factor (FGF)-2. The LMW-H/P MPs-coated matrix with various GFs or cytokines may provide novel biomaterials that can control cellular activity such as growth and differentiation. Thus, LMW-H/P MPs are an excellent carrier for GFs and various cells and are an efficient coating matrix for cell cultures.
Insights
Low-molecular-weight heparin/protamine microparticles (LMW-H/P MPs) effectively carry and protect growth factors and cells. These microparticles enhance cell viability and serve as a versatile coating matrix for cell culture applications.
Area of Science:
- Biomaterials Science
- Cell Biology
- Biotechnology
Background:
- Low-molecular-weight heparin/protamine microparticles (LMW-H/P MPs) are developed as advanced carriers.
- These microparticles are designed to encapsulate heparin-binding growth factors (GFs) and facilitate cell adhesion.
Purpose of the Study:
- To investigate the efficacy of LMW-H/P MPs as a delivery system for GFs and cells.
- To evaluate the potential of LMW-H/P MPs as a biomaterial coating for cell culture and tissue engineering.
Main Methods:
- Production of LMW-H/P MPs by mixing low-molecular-weight heparin and protamine at a 7:3 volume ratio.
- Characterization of microparticle size (0.5-3 µm) and assessment of their binding capabilities to cells and tissue culture plates.
- Evaluation of GF immobilization, controlled release, and activity preservation.
- Assessment of cell viability and aggregate formation upon interaction with LMW-H/P MPs.
Main Results:
- LMW-H/P MPs effectively immobilize, control the release, and protect the activity of GFs.
- Microparticles promote cellular viability through aggregate formation and cell surface binding.
- LMW-H/P MPs demonstrate efficient binding to tissue culture plates, retaining GF binding, including fibroblast growth factor-2 (FGF-2).
Conclusions:
- LMW-H/P MPs serve as an excellent carrier for GFs and various cell types.
- The microparticle-coated matrix offers a novel biomaterial for controlling cellular activities like growth and differentiation.
- LMW-H/P MPs are efficient for cell culture applications, enhancing cell adhesion and viability.
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