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[Comparative study on the pharmacokinetics of rifampicin between the old and middle-aged tuberculosis patients]
1Department of Pharmacology, Tianj in Medical College.
Abstract:
The pharmacokinetics of rifampicin was studied in 16 tuberculosis patients including the elderly (64.3 +/- 4.8 yrs, n = 8) and the middle-aged (35.9 +/- 7.6 yrs, n = 8). 450 mg of rifampicin (RFP) were given orally. The concentration of RFP was assayed by HPLC. The plasma concentration-time curves of both groups fitted to one-compartment model. Important parameters were taken: t 1/2 2.39 +/- 0.66, 3.84 +/- 1.91 h; Cmax: 14.56 +/- 6.45, 9.83 +/- 2.55 micrograms/ml; vd: 0.43 +/- 0.11, 0.67 +/- 0.15L/kg; CL: 0.14 +/- 0.03, 0.13 +/- 0.06 L.h-1/kg respectively. No significant difference was found between the old and middle aged TB patients on the pharmacokinetics of rifampicin (P greater than 0.05). We suggest that 450 mg/day of rifampicin taken orally are available for aging tuberculosis patients.
Insights
Elderly and middle-aged tuberculosis patients showed no significant pharmacokinetic differences when treated with 450 mg of rifampicin (RFP). This oral dosage is considered available for aging individuals with TB.
Area of Science:
- Pharmacology
- Clinical Pharmacy
- Tuberculosis Research
Background:
- Rifampicin (RFP) is a cornerstone antibiotic for tuberculosis (TB) treatment.
- Understanding RFP pharmacokinetics in diverse age groups, including the elderly, is crucial for optimizing TB therapy.
- Age-related physiological changes can potentially alter drug metabolism and elimination.
Purpose of the Study:
- To investigate and compare the pharmacokinetics of oral rifampicin in elderly versus middle-aged tuberculosis patients.
- To determine if age significantly impacts key pharmacokinetic parameters of rifampicin.
- To assess the suitability of standard rifampicin dosing for older TB patients.
Main Methods:
- A comparative pharmacokinetic study involving 16 tuberculosis patients (8 elderly, 8 middle-aged).
- Oral administration of a 450 mg dose of rifampicin (RFP).
- High-performance liquid chromatography (HPLC) was used for RFP plasma concentration analysis.
- One-compartment pharmacokinetic modeling was applied to plasma concentration-time data.
Main Results:
- Plasma concentration-time curves for both groups were best described by a one-compartment model.
- Key pharmacokinetic parameters, including half-life (t 1/2), maximum concentration (Cmax), volume of distribution (vd), and clearance (CL), showed no statistically significant differences between elderly and middle-aged groups (P > 0.05).
- Specific parameters: t 1/2 (2.39 ± 0.66 vs 3.84 ± 1.91 h), Cmax (14.56 ± 6.45 vs 9.83 ± 2.55 µg/ml), vd (0.43 ± 0.11 vs 0.67 ± 0.15 L/kg), CL (0.14 ± 0.03 vs 0.13 ± 0.06 L·h⁻¹·kg⁻¹).
Conclusions:
- The pharmacokinetics of a 450 mg oral dose of rifampicin do not significantly differ between elderly and middle-aged tuberculosis patients.
- Standard oral rifampicin dosing appears to be safe and effective for aging tuberculosis patients.
- This finding supports the use of 450 mg/day rifampicin in the elderly population for tuberculosis treatment.
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