A New Concept in Minimally Invasive Embryo Transfer

Author:

Wieczorek Jarosław1,Stodolak-Zych Ewa2,Okoń Krzysztof3,Koseniuk Jurij4,Bryła Magdalena5,Jura Jacek5,Cegła Mirosław5,Poniedziałek-Kempny Katarzyna5,Rajska Iwona5

Affiliation:

1. University Centre of Veterinary Medicine UJ-UR , Al. Mickiewicza 24/28, 30-059 Kraków , Poland

2. Department of Biomaterials and Composites, Faculty of Materials Science and Ceramics , University of Science and Technology , Al. Mickiewicza 30, 30-059 Kraków , Poland

3. Chair of Pathomorphology, Collegium Medicum , Jagiellonian University , Grzegórzecka 16, 30-332 Kraków , Poland

4. Artvimed Centre for Reproductive Medicine , Legendy 3, 30-147 Kraków , Poland

5. Department of Reproductive Biotechnology and Cryoconservation , National Research Institute of Animal Production , 32-083 Balice n. Kraków , Poland

Abstract

Abstract Considerable variation in embryo transfer (ET) catheter types, diverging opinions on their quality and functionality, complications following the insertion of catheters, low efficiency of the application of ET methods in humans, and their widely varying efficiency in animals demonstrate the need to improve ET methods and to look for new types of catheters. Such an opportunity is offered by the introduction of catheters made of new-generation biomaterials. This study was aimed to introduce a new generation of biomaterials into reproductive biotechnology. New-generation materials were compared with materials that have been used for many years, and the functionality of newly produced catheters was compared in vivo. Five types of biomaterials were tested: polycaprolactone (PCL), dibutyryl chitin (DBC), polypropylene (PP), polyethylene (PE) and polylactide (PLA). The study was carried out in two stages. Firstly, the basic utility parameters such as geometric stability, surface structure and catheter resistance were evaluated. Subsequently, the biocompatibility of selected biomaterials in embryo cultures was examined, and the development potential of the obtained blastocysts was evaluated. In the second stage, in vivo with live animals, the biomaterials were tested for biocompatibility and the obtained catheters were examined for their ET functionality. Efficiency with the use of the newly produced catheters was determined, the quality of the blastocysts obtained after embryo culture in the uterus was assessed, and oviducts were subjected to histopathological examination after embryo transfer. Of the tested biomaterials, only polyethylene (PE) showed adequate biological and material properties and proved suitable for production of ET catheters.

Publisher

Walter de Gruyter GmbH

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