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A sampling system for flowing powders based on the theory of sampling.
Alvarado-Hernández, Barbara B; Sierra-Vega, Nobel O; Martínez-Cartagena, Pedro; Hormaza, Manuel; Méndez, Rafael; Romañach, Rodolfo J.
Afiliação
  • Alvarado-Hernández BB; Department of Chemistry, University of Puerto Rico at Mayaguez, Call Box 9000, Mayaguez 00680, Puerto Rico.
  • Sierra-Vega NO; Department of Chemical Engineering, University of Puerto Rico at Mayaguez, Puerto Rico.
  • Martínez-Cartagena P; Department of Chemistry, University of Puerto Rico at Mayaguez, Call Box 9000, Mayaguez 00680, Puerto Rico.
  • Hormaza M; IBS Caribe INC., P.O. Box 8849, San Juan PR 00910, Puerto Rico.
  • Méndez R; Department of Chemical Engineering, University of Puerto Rico at Mayaguez, Puerto Rico.
  • Romañach RJ; Department of Chemistry, University of Puerto Rico at Mayaguez, Call Box 9000, Mayaguez 00680, Puerto Rico. Electronic address: rodolfoj.romanach@upr.edu.
Int J Pharm ; 574: 118874, 2020 Jan 25.
Article em En | MEDLINE | ID: mdl-31837408
An innovative chute and stream sampler system for flowing powders has been developed and tested. The system is designed for representative sampling based on the principles of the Theory of Sampling (TOS). The sampling system was used in combination with near infrared (NIR) spectroscopy to determine the drug concentration of flowing powders. The system is comprised of three parts: a chute, a stream sampler and a sample collection port. The NIR spectra were obtained at the chute, before entering the sampler, and as the powder flowed through the stream sampler. Samples were also collected from the sample collection port to be analyzed using an ultraviolet-visible (UV-Vis) reference method to determine drug content. A total of eight pharmaceutical powder blends, ranging in concentration from 10.5(%w/w) to 19.5(%w/w) of caffeine, were used to test the sampling system. Materials were characterized before blends were made to provide information on flow properties. The throughput of the system was between 30 and 35 kg/h based on the flow properties of the blend. Drug concentration was effectively determined at the chute and stream sampler. The NIR calibration models showed low root mean squared errors of prediction, 0.65(%w/w) and 0.51(%w/w), for the chute and stream sampler respectively. The NIR calibration models also showed low bias values -0.36(%w/w) at the chute and 0.057(%w/w) at the stream sampler. Significant agreement was obtained between the results from the nondestructive NIR versus the destructive UV-Vis method. Variographic analysis was performed to estimate the analytical and sampling errors when determining the drug concentration at the chute and stream sampler respectively. The variographic analysis showed low analytical errors, 0.103(%w/w)2 and 0.181(%w/w)2 at the chute and stream sampler respectively. The analysis also showed that the minimum practical error (MPE) was around 0.2(%w/w)2 at both chute and stream sampler.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pós Tipo de estudo: Prognostic_studies Idioma: En Revista: Int J Pharm Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Porto Rico País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pós Tipo de estudo: Prognostic_studies Idioma: En Revista: Int J Pharm Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Porto Rico País de publicação: Holanda