Single-Dose Intrapulmonary Pharmacokinetics of Rifapentine in Normal Subjects

Subjects.The protocol was approved by the Human Research Committee of the University of California, San Francisco. Written informed consent was obtained from each subject by an experienced research nurse. Subjects were required to be 18 to 45 years of age. If the subjects were female, they were required to be nonlactating and not pregnant and to agree to use adequate contraception (e.g., barrier methods or abstinence) during the study and for 2 weeks following completion of the study. Women using oral contraceptives were required to agree to use a barrier method in addition for 1 month following the study. Subjects who were lactating or pregnant, had a history of intolerance to rifamycin drugs or topical lidocaine, had clinically significant organ dysfunction, or were required to take chronic medications other than self-prescribed vitamins, birth control pills, or thyroid replacement therapy or who were smoking on a regular basis within 6 months of the study were excluded. Subjects who reported drug or alcohol dependence or who had psychiatric problems that would interfere with participation in the study were also excluded. Twenty subjects were women, and 10 subjects were men. The subjects' age, height, and weight (mean ± standard deviation [SD]) were 29.7 ± 6.2 years, 169 ± 9 cm, and 66.7 ± 13.8 kg, respectively. All subjects had normal renal function as measured by determination of the serum creatinine level (0.8 ± 0.1 mg/dl).

Study design.The investigation was prospective but not randomized or blinded. Thirty normal volunteers divided into six subgroups of five subjects each were assigned to undergo standardized bronchoscopy and bronchoalveolar lavage (BAL) (7, 10) at specified time intervals from 4 to 48 h following oral administration of a single dose of rifapentine. Rifapentine (600 mg) was administered by a research nurse in the Endoscopy Unit, followed by a timed bronchoscopy, as indicated in Table1. All patients were observed for at least 30 min after taking the antibiotic for any signs of an allergic reaction. Bronchoscopy and BAL were performed at 4, 5, 7, 12, 24, and 48 h. Baseline data included the results of a medical history and physical examination; blood tests including a complete blood count with differential and a platelet count and alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, total bilirubin, total protein, albumin, blood urea nitrogen, serum creatinine, and electrolyte level determinations; and urinalysis, including specific gravity, pH, albumin, glucose, ketone, and bilirubin level determinations, and microscopic examination of spun sediment. The postbronchoscopy assessment included a medical history and physical examination, a review of voluntarily described and observed adverse experiences, collection of a sample for antibiotic concentration determination, and a repeat of the laboratory testing of blood and urine. Major adverse reactions were defined as those that were fatal or life-threatening, resulted in permanent disability, required hospitalization, were the result of drug overdose, or suggested significant hazard to the subject.

Bronchoscopy and BAL.Bronchoscopy and BAL were performed in the Endoscopy Unit of the Moffitt-Long Hospitals. The blood pressure, respiratory rate, and heart rate of each subject were recorded before, at the completion of, and at approximately 1 h after bronchoscopy. Oxygenation was monitored by fingertip oximetry throughout the procedure. A 4% topical lidocaine gargle followed by a 4% topical lidocaine spray was used to prepare the subjects for the procedure. Four percent topical lidocaine was then applied to each side of the posterior pharynx, followed by the application of topical 1% lidocaine more distally. Systemic sedation was not used. A fiberoptic bronchoscope (Pentax FB-19H) was inserted into the right middle lobe. The instrument was in place for an average of 4.8 min (range, 3 to 9 min). Four 50-ml aliquots of normal saline were instilled into the right middle lobe, and each was immediately aspirated into a trap.

Specimen handling.All specimens were kept in ice until they were frozen. The blood was centrifuged, and the plasma was separated and then frozen until it was assayed.

Since the BAL fluid aspirated from the first instillation contains significant contamination with cells from the proximal airways (3) it was discarded. The aspirates from the second, third, and fourth instillations were pooled. The volume of the pooled aspirates from the instillations was measured and recorded. Two-milliliter aliquots drawn from the pooled specimens were sent to the clinical laboratory for cell count and differential. Measured volumes were placed in 30-ml polypropylene tubes, and the tubes were immediately spun in a refrigerated centrifuge at 400 × g for 5 min. After separation of the supernatant from the cells, the supernatant was stored at −80°C until assay. The cells were immediately resuspended into 2 ml of acetonitrile with 200 μg of ascorbic acid per ml (acetonitrile/aa) and frozen at −80°C until they were assayed. A small aliquot of each supernatant was frozen separately for urea concentration determination.

Assay for rifapentine concentrations.The rifapentine concentration in plasma was measured by the laboratory at Hoechst Marion Roussel, Inc. (Kansas City, Mo.) by a high-pressure liquid chromatography method that was reported previously (18). Briefly, plasma proteins were precipitated with methanol containing internal standard (25-O-desacetyl rifampin). After centrifugation the supernatant was injected onto a 5-μm Primesphere C₁₈-HC column (2.0 by 150 mm; Phenomenex, Inc., Torrance, Calif.) preceded by a matching guard column. Analytes were eluted with a mobile phase consisting of 40% methanol, 25% acetonitrile, and 35% water containing 0.5% acetic acid. Drug peaks were detected at 480 nm. The validation statement provided by personal communication from an internal research and development report of 5 January 1996 (Marion Merrell Dow Inc., Kansas City, Mo.) stated the following: the assay was validated over the concentration range of 0.5 to 60 μg/ml. Two replicates of seven freshly prepared calibration standards (0, 0.5, 1.0, 15, 30, 45, and 60 μg/ml) and 30 replicates of four validation quality control sample pools (0.5, 1.0, 30, and 60 μg/ml) were assayed in each of three batches run over a period of 2 days. The intraday coefficients of variation ranged from 2.8 to 6.2% for rifapentine and 2.7 to 5.8% for 25-desacetyl rifapentine. The interday coefficients of variation ranged from 0.8 to 4.4% for rifapentine and 0.8 to 5.7% for 25-desacetyl rifapentine. The linearity of the assay (R²) ranged from 0.9993 to 0.9998.

BAL fluid supernatants and ACs were analyzed in the Infectious Diseases Research Laboratory at the University of California, San Francisco. The BAL fluid supernatant was extracted through a Varian (Harbor City, Calif.) Bond Elut C₈ solid-phase extraction column. Diazepam, (Sigma Chemical Co., St. Louis, Mo.) was added to the eluant as an internal standard, and then the eluant was evaporated and resuspended in 200 μl of methanol containing 200 μg of ascorbic acid per ml (methanol/aa). This preparation was injected onto a 5-μm Beckman Ultrasphere octyl column (4.6 mm [inner diameter] by 15 cm). The column was connected to the detector by tubing (polytetrafluoroethylene Teflon; 0.5 mm [inner diameter]) wrapped around a UVP (San Gabriel, Calif.) shortwave Pen-Ray lamp to irradiate the sample. Analytes were detected by measuring the fluorescence at an excitation wavelength of 290 nm and an emission wavelength of 520 nm. The mobile phase consisted of 40% acetonitrile in water, 0.2% phosphoric acid, and 0.5% hydrogen peroxide adjusted to pH 4.5 with sodium hydroxide. Calibration curves and controls were prepared at the same time as the samples.

AC suspensions were prepared as follows. Diazepam was added to the cells suspended in acetonitrile/aa as the internal standard. After centrifugation, the solvent was evaporated and resuspended in 200 μl of methanol/aa. The AC suspensions were then injected onto the system described above. Calibration curves and controls were prepared in acetonitrile on the same day as the samples.

The mean ± SD coefficients of variation for intraday and interday determinations together for rifapentine in BAL fluid supernatants and ACs were 4.91% ± 0.87% and 4.03% ± 1.33%, respectively. For 25-desacetyl rifapentine, they were 7.27% ± 3.40% and 5.48% ± 5.21%, respectively. The linearity of the assay (R²) for rifapentine and 25-desacetyl rifapentine in the BAL fluid supernatants ranged from 0.9950 to 0.9996 and 0.9958 to 0.9994, respectively. For ACs, linearity (R²) ranged from 0.9948 to 0.9998 for rifapentine and from 0.9948 to 0.9994 for 25-desacetyl rifapentine.

Determination of ELF volume and concentration of antibiotics in ELF and ACs.The ELF volume was determined by the urea dilution method (29). The concentration of urea in serum was analyzed by the clinical laboratory at the University of California, San Francisco, by a coupled urease-glutamate dehydrogenase enzymatic method (32) modified by Boehringer Mannheim Corporation (Indianapolis, Ind.). Measurements were made at a fixed time interval that permitted automated analysis with a BM 747 analyzer (Boehringer Mannheim). The urea concentration in the BAL fluid supernatant was measured by a modified enzymatic assay (BUN kit UV-66; Sigma), and the results were read on a Spectronic 20D spectrophotometer (Milton Roy, Rochester, N.Y.). The proportions of the reagent to the specimen were changed from 3.0 ml/0.005 ml, as recommended by the manufacturer, to 2.5 ml/0.5 ml, as reported by Rennard et al. (29). Standard curves prepared in normal saline with concentrations ranging from 0.047 to 0.750 mg/dl were linear (r² ≥ 0.99). Controls with concentrations of 0.094 and 0.375 mg/dl were run with every standard curve used to assay the BAL fluid samples. If the values for the controls were not within 10% of the known value, the standard curve, controls, and BAL fluid sample assays were repeated.

The volume of ELF in BAL fluid was derived from the following relationships:V_ELF = V_BAL × (UREA_BAL/UREA_SER),where V_ELF is volume of ELF sampled by BAL, V_BAL is volume of aspirated BAL fluid; UREA_BAL is the concentration of urea in BAL fluid, and UREA_SER is the concentration of urea in serum. The volume of ACs collected in the pellet suspension was determined from the cell count in the BAL fluid. The cells were counted in a hemocytometer which has a lower detection limit of 1.0 × 10⁶/liter. The number of cells from which drug was extracted was calculated by multiplying the number of cells per milliliter in BAL fluid times the volume (in milliliters) of BAL fluid that was centrifuged to produce the pellet. It has been noted, however, that centrifugation causes an average loss of 21% of the cells (33), so that the actual number of cells recovered postcentrifugation may be less than the number counted, and the actual antibiotic concentration may be proportionately more than we report here. The volume of ACs in the pellet suspension was calculated by using a mean macrophage cell volume of 2.42 μl/10⁶ cells (2). The concentration of antibiotic in alveolar cells, ABX_AC, was calculated from the following relationship (7, 10): ABX_AC = (ABX_PELLET/V_AC) where ABX_PELLET is the antibiotic concentration in the 1-ml cell suspension, and V_AC is the volume of ACs in the 1-ml cell suspension.

Differential cell counting was performed after the specimen was spun in a cytocentrifuge (33).

Statistical analysis and modeling.Statistical analysis and database management were performed by using Prophet, version 6.0 (AbTech Corp., Charlottesville, Va.). Modeling was performed by using Prophet, version 4.1 (BBN, Inc., Cambridge, Mass.), on a Sun 10 Sparc Station (Sun Microsystems, Milpitas, Calif.). The linear regression analysis used the method of least-squares estimation. A Pvalue of <0.05 was regarded as statistically significant. Prior to comparison of the data sets, tests for normality (Wilk-Shapiro test) and equality of variances (Levene's test) were performed. Parametric and nonparametric comparisons were performed by the Neuman-Keuls (all pairwise) or Kruskal-Wallis (unblocked data) and Friedman (blocked data) tests, respectively (34). A P value of <0.05 was regarded as statistically significant.

The intracellular and ELF concentration-time data declined linearly on a logarithmic scale and were fit to a one-compartment model. The plasma concentration-time data were fit to a one-compartment model and a two-compartment model. The log likelihood of the fit, the Schwartz criterion (SC) (30), and the Leonard criterion (LC) (24) were calculated to assess the appropriateness of the two models that were used to fit the concentrations in plasma. SC was derived from the equation SC = log L − (K/2) ln N, where log L was the log likelihood of the fit,K was the number of parameters used in the model, andN was the number of observed concentrations. LC was derived from the equation LC = SC + ½ [K ln (2π N ) + ln(DCM)], where DCM was the determinant of the covariant matrix. SC, LC, the log likelihood of the fit, and the correlation coefficient squared (R²) favored the two-compartment model for the concentrations in plasma. Therefore, this was the model that was used to derive the pharmacokinetic parameters.

The following parameters were estimated from the model: V₁, the volume of distribution of the central compartment; LZ, the elimination rate constant;T_1/2-LZ, the elimination half-life;C_max, the maximum concentration in plasma; andT_max, the time to C_max. Fitting was performed by using a weighting function (1/Y²), where 1/Y is the reciprocal of the observed concentration. The area under the concentration-time curve (AUC) from time zero to infinity (AUC_0–∞) was estimated by noncompartmental analysis by using the log-trapezoidal rule and was extrapolated to infinity by dividing the last predicted concentration by LZ.