Interaction of vitamin B1 and phenylalanine on the pharmacokinetics of ciprofloxacin using bioassay in rabbits


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Authors

  • P ANJANEYULU Sri Venkateswara Veterinary University, Gannavaram, Andhra Pradesh 521 102 India image/svg+xml
  • K V VENKATA RAO Sri Venkateswara Veterinary University, Gannavaram, Andhra Pradesh 521 102 India image/svg+xml
  • SRIVIDYA GULLAPUDI Sri Venkateswara Veterinary University, Gannavaram, Andhra Pradesh 521 102 India image/svg+xml
  • K ASWANI KUMAR Sri Venkateswara Veterinary University, Gannavaram, Andhra Pradesh 521 102 India image/svg+xml
  • V SRI HARSHINI Sri Venkateswara Veterinary University, Gannavaram, Andhra Pradesh 521 102 India image/svg+xml
  • G SAI PRATHYUSHA Sri Venkateswara Veterinary University, Gannavaram, Andhra Pradesh 521 102 India image/svg+xml
  • G S RAO Sri Venkateswara Veterinary University, Gannavaram, Andhra Pradesh 521 102 India image/svg+xml
  • SUMA SRI TIMMAREDDY Sri Venkateswara Veterinary University, Gannavaram, Andhra Pradesh 521 102 India image/svg+xml

https://doi.org/10.56093/ijans.v94i6.147834

Keywords:

Ciprofloxacin, Pharmacokinetics, Phenylalanine, Rabbits, Vitamin B1

Abstract

This pharmacokinetic study was carried out in rabbits following single oral administration of ciprofloxacin to study kinetic behaviour of ciprofloxacin in the presence of vitamin B1 and selected essential amino acid phenylalanine. Rabbits weighing 2-4 kg were randomly assigned to 5 groups of 6 each. Group 1 served as blank without any treatment. Group 2 served as ciprofloxacin control whereas Group 3, 4 and 5 rabbits were co-administered with thiamine (80 mg/kg), phenylalanine (48 mg/kg), combination of thiamine and phenylalanine along with ciprofloxacin (40 mg/kg) orally. Blood samples were collected at predetermined time intervals up to 24 h, and plasma was used for estimation of ciprofloxacin through bioassay. Results obtained from the experiment revealed that rabbits of Group 3, 4 and 5 showed improved levels of Cmax 4.74±0.17, 3.00±0.22, 2.18±0.12 µg/mLand AUC 20.30±5.19, 10.09±1.48, 12.85±1.34 µg.h/mL, respectively when compared to Cmax (2.10±0.14 µg/mL) and AUC (5.90±0.81 µg.h/mL) in Group II rabbits. PK-PD integration of the present study revealed that Cmax: MIC>8, AUC: MIC>125 in Group 3, 4 and 5 implying that the co-administration of vitamin B1 and phenylalanine and their combination improves the antibacterial activity and reduces the development of resistance at the selected dose of ciprofloxacin.

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References

Al-Ghazawi M, Aburjai T, Shraim N, Bani-Jaber A and AbuRuz S. 2012. Effect of Licorice extract on the pharmacokinetics of ciprofloxacin in rabbits after oral administration using an improved high-performance liquid chromatography assay. Jordan Journal of Pharmaceutical Sciences 5(2): 120–30.

Bashir S, Akram M, Qaisar M N and Irfan H M. 2010. Disposition kinetics of ciprofloxacin in normal rabbits and changes observed in induced diabetic condition. Pakistan Journal of Science 62(3): 156–59.

Coates P M, Betz J M, Blackman M R, Cragg G M, Levine M, Moss J and White J D. 2010. Encyclopedia of Dietary Supplements. CRC Press.

Devi K K, Srinu B and Rao G S. 2016. Effect of quercetin on the disposition kinetics of ciprofloxacin. Annals of Phytomedicine 5(2): 103–07.

El-Sayed M G, El-Komy A A, Elbarawy A E and Mustafa G E. 2014. Pharmacokinetical interactions of amoxicillin and amprolium in broiler chickens. Journal of Physiology and Pharmacology Advances 4: 515–24.

Gibaldi M and Perrier D. 1982. A Text Book Onon Pharmacokinetics, 2nd edition. New York: Dekkar.

Grosse W and Wade A E. 1971. The effect of thiamine consumption on liver microsomal drug-metabolizing pathways. Journal of Pharmacology and Experimental Therapeutics 176(3): 758–65.

Lukac M, Lacko I, Bukovsky M, Kyselova Z, Karlovska J, Horvath B and Devinsky F. 2010. Synthesis and antimicrobial activity of a series of optically active quaternary ammonium salts derived from phenylalanine. Open Chemistry 8(1): 194–201.

Ramon J, Dautrey S, Farinoti R, Carbon C and Rubinstein

E. 1994. Intestinal elimination of ciprofloxacin in rabbits.

Antimicrobial Agents and Chemotherapy 38(4): 757–60.

Saadeh A, Aburjai T, Shraim N and Al-Ghazawi M. 2019. The effect of Brassica oleracea (cabbage) on the pharmacokinetics of ciprofloxacin in an animal model. Jordan Journal of Pharmaceutical Sciences 12(2).

Sen F, Ganim M A, Baloglu M C, Aygun A, Sayiner H S, Altunoglu Y C and Bulut E. 2019. Synergistic and antagonistic effects of phenylalanine and various antibiotics on the growth of pathogenic bacteria. BioNanoScience 9: 446–52.

Shaheen H M and El-Sheikh M W. 2011. Pharmacokinetics of ciprofloxacin and its interaction with diclofenac after intravenous injection in healthy rabbits. Kafrelsheikh Veterinary Medical Journal 9(1): 189–209.

Shaheen H M and El-Sheikh M W. 2011. Pharmacokinetics Sharma D, Patel R P, Zaidi S T R, Sarker M M R, Lean Q Y and Ming L C. 2017. Interplay of the quality of ciprofloxacin and antibiotic resistance in developing countries. Frontiers in Pharmacology 8: 546.

Ukpo G E, Owolabi M A, Imaga N O, Oribayo O O and Ejiroghene A J. 2017. Effect of Carica papaya (Linn) aqueous leaf extract on pharmacokinetic profile of ciprofloxacin in rabbits. Tropical Journal of Pharmaceutical Research 16(1): 127–34.

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Submitted

2024-01-27

Published

2024-06-13

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How to Cite

ANJANEYULU, P. ., RAO, K. V. V. ., GULLAPUDI, S. ., KUMAR, K. A. ., HARSHINI, V. S. ., PRATHYUSHA, G. S. ., RAO, G. S. ., & TIMMAREDDY, S. S. . (2024). Interaction of vitamin B1 and phenylalanine on the pharmacokinetics of ciprofloxacin using bioassay in rabbits. The Indian Journal of Animal Sciences, 94(6), 518–521. https://doi.org/10.56093/ijans.v94i6.147834
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