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 | Acesso ao texto completo restrito à biblioteca da Embrapa Instrumentação. Para informações adicionais entre em contato com cnpdia.biblioteca@embrapa.br. |
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Registro Completo |
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Biblioteca(s): |
Embrapa Instrumentação. |
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Data corrente: |
07/02/2025 |
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Data da última atualização: |
07/02/2025 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
ALMEIDA, L. S.; CARNEIRO, J.; COLNAGO, L. A. |
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Afiliação: |
UNIVERSITY OF SAO PAULO; PARANA FEDERAL UNIVERSITY; LUIZ ALBERTO COLNAGO, CNPDIA. |
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Título: |
Time domain NMR for polymorphism characterization: Current status and future perspectives. |
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Ano de publicação: |
2025 |
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Fonte/Imprenta: |
International Journal of Pharmaceutics, v. 669, 125027, 2025. |
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Páginas: |
10 p. |
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ISSN: |
0378-5173 |
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DOI: |
https://doi.org/10.1016/j.ijpharm.2024.125027 |
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Idioma: |
Inglês |
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Conteúdo: |
Polymorphism is the ability of a compound to exist in multiple crystal forms while maintaining the same chemical composition. This phenomenon is reflected in different solid-state physicochemical properties due to variations in structural energy and the degree of lattice disorder. The pharmaceutical industry places significant emphasis on thoroughly characterizing polymorphism in Active Pharmaceutical Ingredients (APIs) because of its impact on the pharmacokinetic properties on the final medicine product. Standard characterization techniques are well documented in pharmacopeias and by international agencies. These techniques, whether applied individually or in combination, include crystallography (X-Ray Diffraction), thermal analysis (Differential Scanning Calorimetry), and various forms of spectroscopy, such as Near-Infrared, Raman, and solid-state Nuclear Magnetic Resonance (NMR). Analyzing NMR applications for solid-state characterization over the past five years, there has been a growing number of reports on the use of Time Domain NMR (TD-NMR) to evaluate polymorphism on APIs. Due to the increasing interest in this compelling technique, this study provides an overview of the current advancements in TD-NMR for polymorphism assessment in pharmaceutical products. Compared to high-field devices, TD-NMR has proven to be more convenient to industrial applications due to its smaller equipment size and shorter measurement times. This mini-review compares various applications of TD-NMR for API solid-state characterization and offer guidance for future research in this area. MenosPolymorphism is the ability of a compound to exist in multiple crystal forms while maintaining the same chemical composition. This phenomenon is reflected in different solid-state physicochemical properties due to variations in structural energy and the degree of lattice disorder. The pharmaceutical industry places significant emphasis on thoroughly characterizing polymorphism in Active Pharmaceutical Ingredients (APIs) because of its impact on the pharmacokinetic properties on the final medicine product. Standard characterization techniques are well documented in pharmacopeias and by international agencies. These techniques, whether applied individually or in combination, include crystallography (X-Ray Diffraction), thermal analysis (Differential Scanning Calorimetry), and various forms of spectroscopy, such as Near-Infrared, Raman, and solid-state Nuclear Magnetic Resonance (NMR). Analyzing NMR applications for solid-state characterization over the past five years, there has been a growing number of reports on the use of Time Domain NMR (TD-NMR) to evaluate polymorphism on APIs. Due to the increasing interest in this compelling technique, this study provides an overview of the current advancements in TD-NMR for polymorphism assessment in pharmaceutical products. Compared to high-field devices, TD-NMR has proven to be more convenient to industrial applications due to its smaller equipment size and shorter measurement times. This mini-review compares various applications of ... Mostrar Tudo |
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Palavras-Chave: |
Active Pharmaceutical Ingredient; NMR; Relaxometry. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 02266naa a2200217 a 4500
001 2172502
005 2025-02-07
008 2025 bl uuuu u00u1 u #d
022 $a0378-5173
024 7 $ahttps://doi.org/10.1016/j.ijpharm.2024.125027$2DOI
100 1 $aALMEIDA, L. S.
245 $aTime domain NMR for polymorphism characterization$bCurrent status and future perspectives.$h[electronic resource]
260 $c2025
300 $a10 p.
520 $aPolymorphism is the ability of a compound to exist in multiple crystal forms while maintaining the same chemical composition. This phenomenon is reflected in different solid-state physicochemical properties due to variations in structural energy and the degree of lattice disorder. The pharmaceutical industry places significant emphasis on thoroughly characterizing polymorphism in Active Pharmaceutical Ingredients (APIs) because of its impact on the pharmacokinetic properties on the final medicine product. Standard characterization techniques are well documented in pharmacopeias and by international agencies. These techniques, whether applied individually or in combination, include crystallography (X-Ray Diffraction), thermal analysis (Differential Scanning Calorimetry), and various forms of spectroscopy, such as Near-Infrared, Raman, and solid-state Nuclear Magnetic Resonance (NMR). Analyzing NMR applications for solid-state characterization over the past five years, there has been a growing number of reports on the use of Time Domain NMR (TD-NMR) to evaluate polymorphism on APIs. Due to the increasing interest in this compelling technique, this study provides an overview of the current advancements in TD-NMR for polymorphism assessment in pharmaceutical products. Compared to high-field devices, TD-NMR has proven to be more convenient to industrial applications due to its smaller equipment size and shorter measurement times. This mini-review compares various applications of TD-NMR for API solid-state characterization and offer guidance for future research in this area.
653 $aActive Pharmaceutical Ingredient
653 $aNMR
653 $aRelaxometry
700 1 $aCARNEIRO, J.
700 1 $aCOLNAGO, L. A.
773 $tInternational Journal of Pharmaceutics$gv. 669, 125027, 2025.
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Embrapa Instrumentação (CNPDIA) |
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| 2. |  | BENITES, V. de M.; MOUTTA, R. de O.; COUTINHO, H. L. da C.; BALIEIRO, F. de C. Análise discriminante de solos sob diferentes usos em área de Mata Atlântica a partir de atributos de matéria orgânica. Revista Árvore, Viçosa, MG, v. 34, n. 4, p. 377-382, 2010.| Tipo: Artigo em Periódico Indexado | Circulação/Nível: B - 1 |
| Biblioteca(s): Embrapa Solos. |
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| 3. | | CUNHA, T. J. F.; MADARI, B. E.; BENITES, V. de M.; CANELLAS, L. P.; NOVOTNY, E. H.; MOUTTA, R. de O.; TROMPOWSKY, P. M.; SANTOS, G. de A. Fracionamento químico da matéria orgânica e características de ácidos húmicos de solos com horizonte a antrópico da Amazônia (Terra Preta). Acta Amazonica, Manaus, v. 37, n. 1, p. 91-98, 2007.| Tipo: Artigo em Periódico Indexado | Circulação/Nível: Nacional - A |
| Biblioteca(s): Embrapa Arroz e Feijão; Embrapa Semiárido; Embrapa Solos. |
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| Registros recuperados : 3 | |
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