The use of a protein source such as serum and albumin had been extensively employed as supplements of culture media for handling and culture of gametes and embryos. Protein molecules behave as colloids in solution and contribute to the osmotic pressure of fluids. The interaction of proteins in solution and spermatozoa needs to be assessed in order to determine their possible role in osmoregulation.
View Article and Find Full Text PDFThe aim of the study was to assess and compare the efficiency of the ZSC-II versus the Sperm Select techniques in preparing human sperm from normozoospermic patients for use in intrauterine insemination and other assisted reproductive technologies. Twenty-five patients were included in the study. Semen was collected at intercourse and processed via 2 sperm preparation methods.
View Article and Find Full Text PDFObjective: Transport of unprocessed human semen specimens from the production site to distant laboratories for andrological evaluation and clinical use requires the development of proper protocols and devices for the shipment and maintenance of sperm viability during transport. Factors such as maintenance of proper temperature and the specific diluent used are considered to affect the viability of semen specimens during transport. The Bio-Tranz shipper (ZDL, Inc.
View Article and Find Full Text PDFObjective: Recent developments in the assisted reproductive technology (ART) areas necessitate the use of new and more efficient and acceptable modes of gamete in vitro manipulation techniques. As established via the use of various forms of ART, the natural process of fertilization has been largely bypassed and the gametes are obtained and manipulated outside of the normal means of conception. For the male, improvements in sperm quality have involved the use of various techniques that aim to recover a small percentage of healthy spermatozoa that can be further used for the different ART procedures.
View Article and Find Full Text PDFThe objective of this study was to develop new techniques for the cryopreservation of washed spermatozoa. Two media (Ham's F-10 and nonthermoprecipitated TEST-yolk buffer [NT-TYB]) containing 7% (v/v) glycerol were compared to semen cryopreservation by adding glycerol directly to the semen. Twenty four men collected a semen specimen each after 4 days of sexual abstinence via the use of a semen collection device at intercourse.
View Article and Find Full Text PDFUse of the media TEST-yolk buffer (TYB) in semenology today enables the short-term incubation and cryostorage of spermatozoa and its subsequent use in the various assisted reproductive technologies (ART). Preparation of TYB media involves the addition of egg yolk (20% v/v) to a physiological solution of the zwitterion buffers TES and Tris. The TYB is usually thermoprecipitated to remove the majority of the egg yolk globules and other macromolecules from the medium.
View Article and Find Full Text PDFObjective: To assess the in vivo efficacy of the tablet drug delivery system containing nonoxynol-9 coprecipitated with polyvinylpyrrolidone by delivering the spermicidal agents vaginally and evaluating their ability to prevent the onset of pregnancy in rabbits.
Design: Controlled clinical study.
Setting: Division of Laboratory and Animal Resources, College of Pharmacy, University of Kentucky.
Objective: To assess whether incubation in TEST-yolk buffer (TYB) or human tubal fluid (HTF) could alter the sperm membrane characteristics and its relationship to antisperm antibodies (ASA) and/or antigen detachment from the sperm membrane and to evaluate the filtration of those specimens and possible recovery of ASA-free spermatozoa.
Design: A prospective clinical study.
Setting: Andrology Institute of Lexington, Lexington, Kentucky.
Objective: To evaluate the effects of cigarette smoking on the ability of seminal plasma (SP) to maintain sperm viability.
Design: Clinical randomized study. Spermatozoa from cigarette smoking or nonsmoking subjects were reconstituted in SP from smokers and nonsmokers and in modified Ham's F-10 medium, followed by sperm quality assessment during a 48-hour incubation period.
The objective of this study was to use the bovine as a model to evaluate the recovery of frozen-thawed spermatozoa via a conventional and a standardized swim-up technique. Frozen-thawed semen specimens (3 bulls) were washed and reconstituted with 2.9% (w/v) sodium citrate extender containing 20% (v/v) chicken egg yolk (SC-EY).
View Article and Find Full Text PDFSperm parameters such as the concentration and percentage of motile spermatozoa are commonly used to assess semen quality. The sperm quality analyzer (SQA) is a device that detects variations in the optical density of motile spermatozoa, providing a sperm motility index (SMI) that is based on various sperm parameters including the concentration, morphology and acrosomal status of motile spermatozoa. The relationship between SMI values of frozen-thawed bovine spermatozoa undergoing swelling in a hypoosmotic medium (100 mOsm/L) and other sperm parameters were evaluated.
View Article and Find Full Text PDFGossypol (GOS) is a polyphenolic compound derived mainly from cottonseed oil, which has been found to have anti-fertility effects in males. It has been reported to induce disturbances of the hypothalamicpituitary axis, disruption of spermatogenesis in the testes, and inhibition of postejaculatory spermatozoa motility. The inhibition of human sperm motility by GOS has been documented both in vivo and in vitro, although the exact mechanism and possible reversibility of such inhibition is unknown.
View Article and Find Full Text PDFThe mouse embryo bioassay (MEB) is a biologically relevant means of quality control (QC) in almost all modes of Assisted Reproductive Technologies (ART). Such QC tests are essential to guarantee that all procedures performed and media used are of adequate quality which would not compromise subsequent pregnancy rates. Although most reports on the use of the MEB for QC in ART laboratories refer to its use in the QC of other parameters such as contact materials, contaminants and environmental parameters of the culture conditions, these same bioassays have been also criticized as not being sensitive enough to suboptimal culture conditions that may affect the outcome of human in-vitro fertilization.
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