CHARACTERIZATION OF PHARMACOKINETICS OF 2-((3-(CHLOROMETHYL)BENZOYL)OXY) BENZOIC ACID IN RATS BY USING HPLC-DAD METHOD

Authors

  • Caroline Faculty of Pharmacy, Widya Mandala Catholic University Surabaya (WMCUS), Indonesia
  • Nathania Sie Faculty of Pharmacy, Widya Mandala Catholic University Surabaya (WMCUS), Indonesia
  • Kuncoro Foe Faculty of Pharmacy, Widya Mandala Catholic University Surabaya (WMCUS), Indonesia
  • Senny Yesery Esar Faculty of Pharmacy, Widya Mandala Catholic University Surabaya (WMCUS), Indonesia
  • Maria Anabella Jessica Faculty of Pharmacy, Widya Mandala Catholic University Surabaya (WMCUS), Indonesia

DOI:

https://doi.org/10.22159/ijap.2019v11i5.34536

Keywords:

2-((3-(Chloromethyl)benzoyl)oxy)benzoic acid, Pharmacokinetics, Rat, HPLC-DAD

Abstract

Objective: A new compound of salicylic acid derivative, namely 2-((3-(chloromethyl)benzoyl)oxy)benzoic acid (3CBB), was synthesized to find a compound exhibiting higher analgesic activity and smaller ulcer irritation than acetylsalicylic acid (ASA). Therefore, this study aimed to investigate the pharmacokinetics of this new compound in rats, following a single dose oral administration of 3CBB (45 mg/kg BW).

Methods: Plasma samples of 9 healthy rats were collected before and up to 3 h after its oral administration, following an 18 h fasting period. Plasma concentrations of 3CBB were determined using a validated HPLC-DAD assay. Pharmacokinetic parameters were determined using the compartment model technique. All experiments were carried out in triplicate.

Results: The pharmacokinetic parameters of 3CBB obtained were as follows: Tmax= 28.9±1.1 min, Cmax = 0.57±0.02 µg/ml, AUCtotal = 66.3±1.0 µg min/ml, Kel = 0.018±0.002 min-1, and T1/2el = 39.4±3.9 min. The long elimination half-life and low Cmax indicated that 3CBB was extensively distributed in the deep and very deep tissues. This confirmed the unique and special characteristics of a highly lipophilic compound like 3CBB (log P = 3.73).

Conclusion: 3CBB demonstrated a slower onset of action and longer elimination time from the body compared to ASA. Thus this new compound is a potential candidate to be developed as a new drug.

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References

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Published

07-09-2019

How to Cite

Caroline, Sie, N., Foe, K., Esar, S. Y., & Jessica, M. A. (2019). CHARACTERIZATION OF PHARMACOKINETICS OF 2-((3-(CHLOROMETHYL)BENZOYL)OXY) BENZOIC ACID IN RATS BY USING HPLC-DAD METHOD. International Journal of Applied Pharmaceutics, 11(5), 279–283. https://doi.org/10.22159/ijap.2019v11i5.34536

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