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LACTEL® 50:50 DL-PLGE, IV 0.95-1.20 is a cost-effective PLGA-based copolymer characterized by its high inherent viscosity of 0.95─1.20 dL/g in HFIP and its controlled degradation period of 6 months.This white to tan pellatized solid is designed for pharmaceutical and medical applications, providing controlled drug release.
LACTEL® 50:50 DL-PLGE, IV 0.95-1.20 is an innovative controlled-release excipient with a polymer composition of 50 mol % D,L-lactide and 50 mol % Glycolide with an ester end group and no added preservatives. As part of Evonik's LACTEL® polymer line, it offers exceptional controlled release of pharmaceutical ingredients in long-acting injectable formulations for veterinary medicine and human generic drug formulations. It is compatible numerous substance types ranging from peptides and proteins to nanoparticles and microparticles. Due to its excellent bioabsorbability it is fully metabolized by the body, offering a degradation period of 6 months with no added preservatives or GMO contents.
Physical state: Solid
Form: Granules
Color: White to light tan
Inherent viscosity (IV) dL/g: 0.95─1.20 (in HFIP)
Degradation time: <6 months
Density (g/mL): 1.34
Tensile Strength (psi): 6000─8000
Elongation (%): 3─10
Modulus (psi): 2─4x10⁵
CAS No. 26780-50-7
Primary Chemistry: Poly(DL-lactide-co-glycolide)
50:50 ratio of D,L-Lactide and Glycolide
Ester end group
6-month degradation time
Biodegradable
Ideal for terminal sterilization
Bioabsorbable excipient
Suitable for use with small molecules, peptides, proteins, and other substances
Non-GMO
No added preservatives
Cost effective
Human generic drug formulations
Long-acting injectable formulations
Price sensitive applications
veterinary medicine
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