Abstract
Background
Cardiomyopathy is a global health crisis that affects people all over the world. Consequently, scientists felt compelled to look for and develop ever-more-powerful pharmaceuticals. For ATTR-CM, the only drug currently recommended by the European Society of Cardiology is Tafamidis.Objectives
The primary aim of this review article is to understand the chemistry, pharmacodynamic, pharmacokinetic, and bio-analytical methods available for Tafamidis.Methods
A systematic review of the existing resources was accomplished up to 2022, comprising existing studies forming the database covering the existing resources from Web of Science, ScienceDirect, and PubMed.Results
The review was based on a systematic review of all the existing studies used to formulate the database. The study also illustrated the PRISMA design that systematically analyses the prevalent resources.Conclusion
Minimal analytical techniques are observed for quantifying the Tafamidis and transthyretin kinetic stabiliser. Therapeutic, pharmacological, and analytical considerations for the novel drug Tafamidis are discussed in this review. Particular attention is paid to the many different analytical and bioanalytical methods currently available for estimating Tafamidis, and the need is highlighted to develop a straightforward, validated technique that meets green chemistry standards.Full text links
Read article at publisher's site: https://doi.org/10.2174/0118715257250153231011062855
References
Articles referenced by this article (37)
Cerebrospinal fluid and vitreous body exposure to orally administered tafamidis in hereditary ATTRV30M (p.TTRV50M) amyloidosis patients.
Amyloid, (2):120-128 2018
MED: 29993288
Tafamidis for autonomic neuropathy in hereditary transthyretin (ATTR) amyloidosis: a review.
Clin Auton Res, (Suppl 1):19-24 2019
MED: 31407119
Specific Therapy for Transthyretin Cardiac Amyloidosis: A Systematic Literature Review and Evidence-Based Recommendations.
J Am Heart Assoc, (19):e016614 2020
MED: 32969287
Cost-Effectiveness of Tafamidis Therapy for Transthyretin Amyloid Cardiomyopathy.
Circulation, (15):1214-1224 2020
MED: 32078382
Pharmacological treatment for familial amyloid polyneuropathy.
Cochrane Database Syst Rev, CD012395 2020
MED: 32311072
Overview of treatments used in transthyretin-related hereditary amyloidosis: a systematic review.
Eur J Hosp Pharm, (4):194-201 2019
MED: 32587078
Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy.
J Neurol, (11):2802-2814 2013
MED: 23974642
Influence of baseline neurologic severity on disease progression and the associated disease-modifying effects of tafamidis in patients with transthyretin amyloid polyneuropathy.
Orphanet J Rare Dis, (1):225 2018
MED: 30558645
Tafamidis for transthyretin familial amyloid polyneuropathy: a randomized, controlled trial.
Neurology, (8):785-792 2012
MED: 22843282
Pathophysiology and Therapeutic Approaches to Cardiac Amyloidosis.
Circ Res, (10):1554-1575 2021
MED: 33983835
Show 10 more references (10 of 37)
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