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1.
Eur J Pharm Biopharm ; 201: 114345, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38823540

ABSTRACT

This study evaluated the synthesis of protic ionic liquids (PILs), 2-hydroxy ethylammonium formate (2-HEAF) and 2-hydroxy ethylammonium acetate (2-HEAA), and their applicability in the crystallization process of the active pharmaceutical ingredient isoniazid (INH) as anti-solvent. Isoniazid is an antibiotic used in the treatment of tuberculosis infections, being used as a first-line chemotherapeutic agent against Mycobacterium tuberculosis. Futhermore, this investigation was conducted in order to evaluate how these PILs can influence the habit, solubility, stability, and therapeutic efficiency of the obtained isoniazid crystals. The 2-HEAF and 2-HEAA PILs were easily formed in reactions between ethanolamine and carboxylic acids (formic or acetic acid), and they have no toxicity against Artemia salina. The PILs were able to crystallize isoniazid, influencing the crystal habit and size. The greatest variations in the hydrogen signals of the NH2 and NH groups of the amine and low variations in the chemical shifts of the hydrogens of the cation of the ethanolamine group from 2-HEAA and 2-HEAF indicate that PILs establish possibly weak interactions with INH. The obtained crystals were amorphous and showed higher solubility in water than standard INH. Moreover, these crystals showed therapeutic efficiency inantimycobacterial activity to inhibit the growth of Mycobacterium tuberculosis. The INH:2-HEAF only degraded 5.1 % (w/w), however, INH:2-HEAA degraded 32.8 % (w/w) after 60 days in an accelerated atmosphere. Then, the 2-HEAA and 2-HEAF were able to crystallize isoniazid, being a new application for these PILs. The used PILs also influenced the characteristics of isoniazid crystals.


Subject(s)
Antitubercular Agents , Crystallization , Ionic Liquids , Isoniazid , Solubility , Isoniazid/chemistry , Isoniazid/pharmacology , Antitubercular Agents/pharmacology , Antitubercular Agents/chemistry , Ionic Liquids/chemistry , Animals , Artemia/drug effects , Mycobacterium tuberculosis/drug effects , Green Chemistry Technology/methods , Drug Stability
2.
Bioresour Technol ; 224: 694-701, 2017 Jan.
Article in English | MEDLINE | ID: mdl-27864129

ABSTRACT

To enhance the enzymatic digestibility of cashew apple bagasse (CAB) feedstock in order to produce sugar fermentation-derived bioproducts, the CAB was subjected to three different pretreatments with the ionic liquid 2-hydroxyl-ethylammonium acetate (2-HEAA) and characterized by FTIR, NMR and chemical methods. All conditions were able to delignify CAB, however the best lignin removal (95.8%) was achieved through the method performed with 8.7% w/w of CAB/2-HEAA ratio at 130°C for 24h. Although the cellulose crystallinity has been increased in CAB treated with the ionic liquid, but this fact did not influence its digestibility. Nevertheless, the pretreatment with 2-HEAA enhanced significantly the cellulose digestibility, increasing the glucose yield from 48 to 747.72mgglucose/gCAB. Furthermore, 2-HEAA pretreatment was efficient even with reused ionic liquid, obtaining high glucose concentration.


Subject(s)
Anacardium/chemistry , Biotechnology/methods , Ionic Liquids/chemistry , Acetates/chemistry , Anacardium/metabolism , Cellulase/chemistry , Cellulase/metabolism , Cellulose/chemistry , Cellulose/metabolism , Ethanolamine/chemistry , Glucose/chemistry , Glucose/metabolism , Hydrolysis , Industrial Waste , Lignin/chemistry , Magnetic Resonance Spectroscopy , Spectroscopy, Fourier Transform Infrared
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