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Mass Spectrometry in Pharmacokinetic Studies of a Synthetic Compound for Spinal Cord Injury Treatment.

BioMed research international (2015-06-20)
María Sánchez-Sierra, Isabel García-Álvarez, Alfonso Fernández-Mayoralas, Sandra Moreno-Lillo, Gemma Barroso García, Verónica Moral Dardé, Ernesto Doncel-Pérez
RESUMEN

The studies of drugs that could constitute a palliative to spinal cord injury (SCI) are a continuous and increasing demand in biomedicine field from developed societies. Recently we described the chemical synthesis and antiglioma activity of synthetic glycosides. A synthetic sulfated glycolipid (here IG20) has shown chemical stability, solubility in polar solvents, and high inhibitory capacity over glioma growth. We have used mass spectrometry (MS) to monitor IG20 (m/z = 550.3) in cells and tissues of the central nervous system (CNS) that are involved in SCI recovery. IG20 was detected by MS in serum and homogenates from CNS tissue of rats, though in the latter a previous deproteinization step was required. The pharmacokinetic parameters of serum clearance at 24 h and half-life at 4 h were determined for synthetic glycoside in the adult rat using MS. A local administration of the drug near of spinal lesion site is proposed.

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Alcohol etílico puro, 200 proof, anhydrous, ≥99.5%
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Alcohol etílico puro, 190 proof, ACS spectrophotometric grade, 95.0%
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Alcohol etílico puro, 190 proof, meets USP testing specifications
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Diisopropyl ether, anhydrous, 99%, contains either BHT or hydroquinone as stabilizer
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Etanol, ≥99.5%, suitable for HPLC
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Etanol, JIS 1000, ≥99.5%, suitable for residue analysis
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Etanol, JIS 300, ≥99.5%, suitable for residue analysis