Quantitative evaluation of the thallium binding of soluble and insoluble Prussian blue hexacyanoferrate analogs: A scientific comparison based on their critical quality attributes.

Hexacyanoferrate Maximal binding capacity (MBC) Moisture content Particle size Product quality Prussian blue Thallium binding

Journal

International journal of pharmaceutics
ISSN: 1873-3476
Titre abrégé: Int J Pharm
Pays: Netherlands
ID NLM: 7804127

Informations de publication

Date de publication:
05 Oct 2019
Historique:
received: 10 04 2019
revised: 01 08 2019
accepted: 03 08 2019
pubmed: 12 8 2019
medline: 28 1 2020
entrez: 12 8 2019
Statut: ppublish

Résumé

There has been a long-standing discussion in the scientific literature on the thallium (Tl) binding capacity of ferric hexacyanoferrate (insoluble) and potassium hexacyanoferrate (soluble) forms of Prussian blue (PB). The literature sometime suggests that the soluble form of PB should be used to treat thallium poisoning, instead of the FDA approved insoluble form of PB. The literature debate is further complicated by the lack of fundamental characterization data such as critical quality attributes (CQAs) that clearly define the analog forms. The purpose of this study is to compare, the binding capacity of soluble and insoluble PB analogs with the same CQAs (particle size/distribution and water content). Water content and particle size/particle distribution were determined by TGA, and solid-state laser diffraction particle sizing. Thallium binding studies were conducted at physiological pH to determine the maximal binding capacity (MBC) at equilibrium. Multiple linear regression and principal component analysis was also used for multivariate data analysis. Results indicate that insoluble and soluble analogs, with similar quality attributes, have nearly identical, MBC binding capacities of (441.5 mg/g) for insoluble vs soluble (458.4 mg/g). However, when both analog forms with different CQAs such as water, particle size were compared, results indicated significantly higher or lower thallium binding levels. In conclusion, it is essential that the FDA approved iron form with well-defined CQAs is used to treat thallium poisoning and radioactive thallium metal contamination for consistent therapeutic outcomes.

Identifiants

pubmed: 31401298
pii: S0378-5173(19)30645-3
doi: 10.1016/j.ijpharm.2019.118600
pii:
doi:

Substances chimiques

Antidotes 0
Ferrocyanides 0
Water 059QF0KO0R
Thallium AD84R52XLF
ferric ferrocyanide TLE294X33A

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

118600

Informations de copyright

Published by Elsevier B.V.

Auteurs

Patrick J Faustino (PJ)

Food and Drug Administration, Center for Drug Evaluation and Research, Office of Testing and Research, Division of Product Quality Research, Life Science Building-64, 10903 New Hampshire Ave., Silver Spring, MD 20993, United States.

Andrew Brown (A)

Department of Chemistry, Texas A & M University, PO Box 30012, College Station, TX 77842, United States.

Bryan Lowry (B)

Food and Drug Administration, Center for Drug Evaluation and Research, Office of Testing and Research, Division of Product Quality Research, Life Science Building-64, 10903 New Hampshire Ave., Silver Spring, MD 20993, United States.

Yongsheng Yang (Y)

Food and Drug Administration, Center for Drug Evaluation and Research, Office of Testing and Research, Division of Product Quality Research, Life Science Building-64, 10903 New Hampshire Ave., Silver Spring, MD 20993, United States.

Yifan Wang (Y)

Food and Drug Administration, Center for Drug Evaluation and Research, Office of Testing and Research, Division of Product Quality Research, Life Science Building-64, 10903 New Hampshire Ave., Silver Spring, MD 20993, United States.

Mansoor A Khan (MA)

Food and Drug Administration, Center for Drug Evaluation and Research, Office of Testing and Research, Division of Product Quality Research, Life Science Building-64, 10903 New Hampshire Ave., Silver Spring, MD 20993, United States; Irma Rangel College of Pharmacy, Texas A & M University, College Station, TX 77843, United States.

Kim R Dunbar (KR)

Department of Chemistry, Texas A & M University, PO Box 30012, College Station, TX 77842, United States.

Adil Mohammad (A)

Food and Drug Administration, Center for Drug Evaluation and Research, Office of Testing and Research, Division of Product Quality Research, Life Science Building-64, 10903 New Hampshire Ave., Silver Spring, MD 20993, United States. Electronic address: adil.mohammad@fda.hhs.gov.

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Classifications MeSH