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LACTEL® 75:25 DL-PLGE, IV 0.55-0.75 is an unpurified bioresorbable polymer that offers a cost-effective excipient solution for controlled drug release systems in pharmaceutical and medical applications. It exhibits inherent viscosity of 0.55─0.75 dL/g in HFIP and a degradation time of 6 months maximum.
LACTEL® 75:25 DL-PLGE, IV 0.55-0.75 is a non-GMO pharmaceutical excipient with a polymer composition of 75 mol % D,L-lactide and 25 mol % Glycolide with an ester end group and no added preservatives. Formulated with 100% bioresorbability, it is fully metabolized by the body for exceptional effectiveness allowing for controlled drug release and a degredation period of 6 months. LACTEL® 75:25 DL-PLGE, IV 0.55-0.75 should be used in the formulation of veterinary medicine and human generic drug formulations.
Physical state: Solid
Form: Granules or pellets
Color: White to yellowish, off-white to light tan
Inherent viscosity (IV) dL/g: 0.55─0.75 (in chloroform)
Degradation time: <6 months
Crystalline Melt Transition (°C): Amorphous
Glass transition temp (°C): 50─55
Solubility (@ 5% w/w): Dichloromethane, tetrahydrofuran, ethyl acetate, chloroform, hexafluoroisopropanol, acetone
Approx. resorption (months): 4─5
Density (g/mL): 1.30
Tensile Strength (psi): 6000─8000
Elongation (%): 3─10
Modulus (psi): 2─4x10⁵
CAS No. 26780-50-7
Primary Chemistry: Poly(DL-lactide-co-glycolide)
Human generic drug formulations Long-acting injectable formulations Price sensitive applications veterinary medicine
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