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dc.contributor.author
Brevedan, Marta Ingrid Victoria  
dc.contributor.author
Varillas, María Alejandra  
dc.contributor.author
González Vidal, Noelia Luján  
dc.date.available
2023-11-10T16:05:50Z  
dc.date.issued
2022-11  
dc.identifier.citation
Brevedan, Marta Ingrid Victoria; Varillas, María Alejandra; González Vidal, Noelia Luján; Influence of storage conditions on pharmaceutical equivalence and similarity of hydrochlorothiazide tablets; Dissolution Technologies, Inc; Dissolution Technologies; 29; 4; 11-2022; 1-9  
dc.identifier.issn
1521-298X  
dc.identifier.uri
http://hdl.handle.net/11336/217803  
dc.description.abstract
Similarity studies are used with the intention to establish interchangeability of certain formulations in vitro, without the need to carry out in vivo studies. This interchangeability between formulations should be conserved during the product shelf life, as an integral part of the pharmaceutical stability. Hydrochlorothiazide (HCTZ), a widely used diuretic, is classified as a class 3 drug in the Biopharmaceutics Classification System (BCS). An immediate-release (IR) solid oral formulation containing a class 3 drug is a candidate for biowaiver if it meets the requirement of ῾very rapid dissolution’ (i.e., ≥ 85% dissolved within 15 minutes). This research aimed to compare four solid oral IR HCTZ formulations (50 mg), commercially available in Argentina, with respect to pharmaceutical similarity and stability. To assess for similarity, dissolution profiles were compared both at time zero (T0) and after 12 months of storage (T12) at pH 1.2, 4.5, and 6.8. To assess for stability, critical quality attributes (CQAs) of the samples were evaluated at T12 of storage (25 °C, 60% relative humidity). At T12, all samples met the requirements for CQAs (i.e., assay, friability, disintegration, uniformity, and dissolution). The reference formulation had the fastest dissolution rate, and sample D was the slowest. Two multisource formulations exhibited statistical differences with respect to the reference sample, both at T0 and T12. Because the evaluated multisource formulations did not meet criteria for very rapid dissolution, they are not candidates for biowaivers. In terms of stability, some statistical differences were detected between dissolution performance at T0 and T12 (for some samples and dissolution media), but no specific pattern could be detected. Thus, it can be considered that the storage conditions did not affect the critical quality attributes of evaluated samples, and their pharmaceutical equivalence was maintained.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Dissolution Technologies, Inc  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
BIOWAIVER  
dc.subject
CRITICAL QUALITY ATTRIBUTES  
dc.subject
DISSOLUTION  
dc.subject
HYDROCHLOROTHIAZIDE (HCTZ)  
dc.subject
STABILITY  
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STORAGE  
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Otras Ingenierías y Tecnologías  
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Otras Ingenierías y Tecnologías  
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INGENIERÍAS Y TECNOLOGÍAS  
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Otras Ciencias de la Salud  
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Ciencias de la Salud  
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CIENCIAS MÉDICAS Y DE LA SALUD  
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Química Analítica  
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Ciencias Químicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Influence of storage conditions on pharmaceutical equivalence and similarity of hydrochlorothiazide tablets  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2023-11-09T14:55:55Z  
dc.journal.volume
29  
dc.journal.number
4  
dc.journal.pagination
1-9  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Hockessin  
dc.description.fil
Fil: Brevedan, Marta Ingrid Victoria. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina  
dc.description.fil
Fil: Varillas, María Alejandra. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina  
dc.description.fil
Fil: González Vidal, Noelia Luján. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina  
dc.journal.title
Dissolution Technologies  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://dissolutiontech.com/issues/202211/HCTZ.pdf  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.14227/DT290422PGC1