Snapshots of Iron Speciation: Tracking the Fate of Iron Nanoparticle Drugs via a Liquid Chromatography–Inductively Coupled Plasma–Mass Spectrometric Approach-Reference-Cited by-同舟云学术

Snapshots of Iron Speciation: Tracking the Fate of Iron Nanoparticle Drugs via a Liquid Chromatography–Inductively Coupled Plasma–Mass Spectrometric Approach

Published:2019-01-24 Issue:3 Volume:16 Page:1272-1281
ISSN:1543-8384
Container-title:Molecular Pharmaceutics
language:en
Short-container-title:Mol. Pharmaceutics

Author:

Neu Heather M.¹,Alexishin Sergei A.¹,Brandis Joel E. P.¹,Williams Anne M. C.¹,Li Wenjing¹,Sun Dajun²,Zheng Nan²,Jiang Wenlei²,Zimrin Ann³,Fink Jeffrey C.⁴,Polli James E.¹^ORCID,Kane Maureen A.¹,Michel Sarah L. J.¹^ORCID

Affiliation:

1. Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland 21201, United States

2. Office of Research and Standards, Office of Generic Drugs, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland 20993, United States

3. Oncology Program, University of Maryland School of Medicine, Baltimore, Maryland 21201, United States

4. Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland 21201, United States

Funder

U.S. Food and Drug Administration

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Pharmaceutical Science,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.molpharmaceut.8b01215

Reference51 articles.

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3. Gottlieb, S. Reducing the Hurdles for Complex Generic Drug Development. FDA Voice, 2017, https://blogs.fda.gov/fdavoice/index.php/2017/10/reducing-the-hurdles-for-complex-generic-drug-development/.

4. Equivalence and regulatory approaches of nonbiological complex drug products across the United States, the European Union, and Turkey

5. Equivalence of complex drug products: advances in and challenges for current regulatory frameworks

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