Impact of lactoferrin supplementation on cotrimoxazole pharmacokinetics: A preliminary clinical investigation
Background and Purpose: Cotrimoxazole, a commonly prescribed antibiotic, has substantial resistance, especially in Indonesia, with its uropathogenic resistance reaching 67% in 2017. Although cotrimoxazole has been suggested to be co-administered with lactoferrin to enhance its antibacterial effectiv...
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International Association of Physical Chemists (IAPC),
2024-06-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_8be0eaa7c81d45a88aa31dbfeba5d6d0 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Dion Notario |e author |
700 | 1 | 0 | |a Angela Marietha Munzir |e author |
700 | 1 | 0 | |a Yulina Novella |e author |
700 | 1 | 0 | |a Linawati Hananta |e author |
245 | 0 | 0 | |a Impact of lactoferrin supplementation on cotrimoxazole pharmacokinetics: A preliminary clinical investigation |
260 | |b International Association of Physical Chemists (IAPC), |c 2024-06-01T00:00:00Z. | ||
500 | |a 10.5599/admet.2358 | ||
500 | |a 1848-7718 | ||
520 | |a Background and Purpose: Cotrimoxazole, a commonly prescribed antibiotic, has substantial resistance, especially in Indonesia, with its uropathogenic resistance reaching 67% in 2017. Although cotrimoxazole has been suggested to be co-administered with lactoferrin to enhance its antibacterial effectiveness and this practice has been widely adopted since the Covid-19 pandemic, the impact of lactoferrin on the pharmacokinetics of cotrimoxazole remains relatively unknown. This study aims to conduct a preliminary clinical investigation into the impact of lactoferrin supplementation on the pharmacokinetics of cotrimoxazole, focusing on the elimination rate and excretion of unchanged drug in urine. Experimental Approach: This study employed a blinded, cross-over, single-dose pharmacokinetics investigation, which included five healthy volunteers as participants. In the initial period, the first group received cotrimoxazole (80 mg trimethoprim and 400 mg sulfamethoxazole) along with a lactoferrin-containing supplement, while the second group only received cotrimoxazole. Subsequently, after a washout period, the conditions were reversed. Urine sampling was conducted at intervals from 0 to 24 hours post-medication, and drug levels in the urine were determined using high-performance liquid chromatography. Key Results: The population-based pharmacokinetic analysis revealed that the optimal model was the one-compartment model with first-order elimination and proportional residual error. Conclusion: The findings show that the administration of lactoferrin-containing supplements did not significantly influence the covariate model and, therefore, did not alter the pharmacokinetics parameter of cotrimoxazole in urine with a single administration, implying that lactoferrin did not cause drug interaction problems when given simultaneously. | ||
546 | |a EN | ||
690 | |a population pharmacokinetics | ||
690 | |a urinary excretion | ||
690 | |a one-compartment | ||
690 | |a drug interaction | ||
690 | |a Therapeutics. Pharmacology | ||
690 | |a RM1-950 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n ADMET and DMPK (2024) | |
787 | 0 | |n https://pub.iapchem.org/ojs/index.php/admet/article/view/2358 | |
787 | 0 | |n https://doaj.org/toc/1848-7718 | |
856 | 4 | 1 | |u https://doaj.org/article/8be0eaa7c81d45a88aa31dbfeba5d6d0 |z Connect to this object online. |