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Preparation, characterization and application of long-acting FSH analogs for assisted reproduction
- Source :
- Theriogenology. 112:11-17
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
Abstract
- Assisted reproduction technologies are widely used in humans and domestic animals and often include follicle stimulating hormone (FSH) in the protocol. One limitation with most of the available FSH preparations is the relative short half-life in the circulation that dictates multiple daily injections for the desired follicle development and superovulation. The development of bioactive long-acting structurally modified FSH analogs is desirable for human and veterinary use. In addition, optimal preparations and/or formulations are expected to improve the regimen and efficiency of the treatment. This review briefly describes the approaches that have been explored to extend the half-life of FSH in the circulation. These include strategies to increase the mass and/or charge of FSH and to prevent the dissociation of the hormone to inactive subunits components. Most of these strategies, except one that led to a registered drug (Elonva) indicated for controlled ovarian stimulation protocols in humans, are still in experimental stage.
- Subjects :
- 0301 basic medicine
Drug
endocrine system
medicine.medical_specialty
Reproductive Techniques, Assisted
media_common.quotation_subject
Superovulation
Stimulation
Biology
Protein Engineering
Polyethylene Glycols
03 medical and health sciences
Follicle
Follicle-stimulating hormone
Ovulation Induction
Food Animals
Internal medicine
medicine
Animals
Humans
Small Animals
media_common
Equine
030104 developmental biology
Endocrinology
Long acting
Animals, Domestic
Drug Design
Female
Animal Science and Zoology
Follicle Stimulating Hormone
Reproduction
Half-Life
Hormone
Subjects
Details
- ISSN :
- 0093691X
- Volume :
- 112
- Database :
- OpenAIRE
- Journal :
- Theriogenology
- Accession number :
- edsair.doi.dedup.....d96f063a39ddb7ea5e51b2692f5835f1
- Full Text :
- https://doi.org/10.1016/j.theriogenology.2017.08.020