Standardisation of Microencapsulation Protocol for Cryopreservation of Malabari Goat Semen

Authors

  • Kiran Mariya George Department of Animal Reproduction, Gynaecology and Obstetrics, College of Veterinary and Animal Sciences, Kerala Veterinary and Animal Science University, Kerala, India
  • Bahuleyan Bibin Becha Base Farm, Kolahalamedu, Idukki, Kerala, India
  • Melitta Pappu Unnikrishnan Centre for Pig Production and Research College of Veterinary and Animal Sciences, Kerala Veterinary and Animal Science University, Kerala, India
  • Choppillil Jayakumar Department of Animal Reproduction, Gynaecology and Obstetrics, College of Veterinary and Animal Sciences, Kerala Veterinary and Animal Science University, Kerala, India
  • Suresh Narayanan Nair Department of Veterinary Pharmacology and Toxicology College of Veterinary and Animal Sciences, Kerala Veterinary and Animal Science University, Kerala, India
  • Leena Chandrasekhar Department of Veterinary Anatomy College of Veterinary and Animal Sciences, Kerala Veterinary and Animal Science University, Kerala, India

DOI:

https://doi.org/10.48165/ijar.2025.46.01.9

Keywords:

Semen evaluation, Microencapsulation, Alginate, Microcapsule, Malabari, Goat

Abstract

The study was conducted to characterise fresh semen and to standardise a microencapsulation protocol for cryopreser vation of Malabari buck spermatozoa. Fresh semen evaluation revealed the ejaculate volume (1.10 ± 0.24 ml), progressive motility (87.50 ± 2.14 %), concentration of spermatozoa (3829.16 ± 172.01 million/mL), viability (92.16 ± 1.62 %), mor phological abnormalities (1.91 ± 0.23 %), functional membrane integrity (64.00 ± 1.93 %) and acrosome integrity (93.16 ± 1.01 %) within normal range. Pooled good quality ejaculates from bucks with good semen freezability were extended in Tris egg yolk based extender; microcapsules were prepared after mixing with sodium alginate at different concentra tions (2.5% and 3%), at different ratios of alginate and extended semen (1:0.6 and 1:1) and extruding through different sizes of hypodermic needle (22 G, 23 G and 24 G) to obtain microcapsules of different size and shape. The size, shape and wall integrity of microcapsules were evaluated in all combinations of production parameters. Alginate concentration of 3 per cent, when mixed with extended semen at the ratio 1:1 and extruded through a 24 G needle into a five per cent barium chloride solution at a fixed distance of 3 cm from the needle tip yielded globular, 1.7 mm sized capsules with 65 per cent wall integrity.

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thesis submitted to Kerala Veterinary and Animal Sciences University, Pookode, Kerala, India.

Sultana, F., Husain, S.S., Khatun, A., Apu, A.S. and Khandoker, M.A.M.Y. (2013). Study on buck evaluation based on semen quality and fertility. Bangladesh J. Anim. Sci.,42: 101-108.

Tamuli, M.K. and Watson, P.F. (1994). Use of a simple staining technique to distinguish acrosomal changes in the live sperm sub-population. Anim. Reprod. Sci., 35: 247-254.

Torre, M.L., Faustini, M., Norberti, R., Stacchezzini, S., Maggi, L., Maffeo, G., Conte, U. and Vigo, D. (2002). Boar semen-con

trolled delivery system: storage and in vitro spermatozoa release. J. Control. Release., 85: 83-89.

Urmila, S. (2022). Freezability and in vitro fertility of Malabari buck semen cryopreserved in liposome-based extender. M.V.Sc. thesis submitted to Kerala Veterinary and Animal Sciences University, Pookode, Kerala, India.

Weber, W., Rimann, M., Schafroth, T., Witschi, U. and Fussenegger, M. (2006). Design of high-throughput-com patible protocols for microencapsulation, cryopreservation and release of bovine spermatozoa. J. Biotech., 123: 155-163.

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Published

2025-04-14

How to Cite

George, K.M., Becha, B.B., Unnikrishnan, M.P., Jayakumar, C., Nair, S.N., & Chandrasekhar, L. (2025). Standardisation of Microencapsulation Protocol for Cryopreservation of Malabari Goat Semen . The Indian Journal of Animal Reproduction, 46(1), 54–60. https://doi.org/10.48165/ijar.2025.46.01.9