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Pharmacokinetics of mefloquine and its effect on sulfamethoxazole and trimethoprim steady-state blood levels in intermittent preventive treatment (IPTp) of pregnant HIV-infected women in Kenya
© Green et al. 2015
- Received: 4 June 2015
- Accepted: 12 December 2015
- Published: 5 January 2016
Intermittent preventive treatment in pregnancy with sulfadoxine/pyrimethamine is contra-indicated in HIV-positive pregnant women receiving sulfamethoxazole/trimethoprim prophylaxis. Since mefloquine is being considered as a replacement for sulfadoxine/pyrimethamine in this vulnerable population, an investigation on the pharmacokinetic interactions of mefloquine, sulfamethoxazole and trimethoprim in pregnant, HIV-infected women was performed.
A double-blinded, placebo-controlled study was conducted with 124 HIV-infected, pregnant women on a standard regimen of sulfamethoxazole/trimethoprim prophylaxis. Seventy-two subjects received three doses of mefloquine (15 mg/kg) at monthly intervals. Dried blood spots were collected from both placebo and mefloquine arms four to 672 h post-administration and on day 7 following a second monthly dose of mefloquine. A novel high-performance liquid chromatographic method was developed to simultaneously measure mefloquine, sulfamethoxazole and trimethoprim from each blood spot. Non-compartmental methods using a naïve-pooled data approach were used to determine mefloquine pharmacokinetic parameters.
Sulfamethoxazole/trimethoprim prophylaxis did not noticeably influence mefloquine pharmacokinetics relative to reported values. The mefloquine half-life, observed clearance (CL/f), and area-under-the-curve (AUC0→∞) were 12.0 days, 0.035 l/h/kg and 431 µg-h/ml, respectively. Although trimethoprim steady-state levels were not significantly different between arms, sulfamethoxazole levels showed a significant 53 % decrease after mefloquine administration relative to the placebo group and returning to pre-dose levels at 28 days.
Although a transient decrease in sulfamethoxazole levels was observed, there was no change in hospital admissions due to secondary bacterial infections, implying that mefloquine may have provided antimicrobial protection.
In many parts of Africa, pregnancy is complicated by co-infection with malaria and human immunodeficiency virus (HIV). Maternal malaria was associated with a two-fold higher HIV-1 viral concentration, and in areas where HIV prevalence is greater than 10 % of the population, the proportional increase of malaria during pregnancy can be from 5.5 to 18.8 % . Some reports show that malaria increases the incidence of mother-to-child HIV transmission as well as contributing to low birth weight and maternal anaemia [1, 2]. In addition, drugs used to treat HIV and associated infections may cause serious drug interactions. For example, HIV-infected patients receiving co-trimoxazole (sulfamethoxazole/trimethoprim) prophylaxis should not take another sulfonamide-containing drug, such as sulfadoxine/pyrimethamine (SP), as the risk of sulfonamide-induced adverse effects is increased. Since physiological functions are altered during pregnancy, the pharmacokinetics of many anti-malarials are different in pregnant women compared to non-pregnant women [3–5].
The only drug currently recommended for malaria intermittent preventive treatment (IPTp) during pregnancy is SP . The development of resistance to SP, as well as safety concerns, has limited the options for malaria prevention in pregnant women [7–9]. The Global Malaria-in-Pregnancy Consortium aims to identify alternatives to SP for IPTp, and has considered mefloquine (MQ) as a potential replacement for SP-IPTp. Although MQ has been used for treatment of multidrug-resistant Plasmodium falciparum infections since the 1960s, there have been few MQ pharmacokinetic studies involving pregnant women. Pharmacokinetic parameters of many drugs are altered in pregnant women due to the differences in the physiological functions relative to non-pregnant women. For example, a controlled study of pregnant and non-pregnant women infected with P. falciparum showed a significantly lower maximum blood concentration (Cmax) and a larger volume of distribution (Vd/F) of MQ in the pregnant group . In addition, interactions with other medications commonly used as prophylaxis against opportunistic infections in HIV-infected individuals may influence MQ pharmacokinetics.
The effects of various drugs on co-trimoxazole (CTX) levels and the effects of CTX on certain drug levels have been assessed in numerous studies. Co-administration of lamivudine with CTX resulted in an increased drug exposure and decreased clearance of lamivudine  while disposition of indinavir , maraviroc  or zidovudine  was not affected by co-administration with CTX. Rifampicin was shown to reduce both trimethoprim and sulfamethoxazole concentrations in HIV-infected patients . To date, there are no data on the interaction between CTX and MQ.
A multicentre, randomized, placebo-controlled, clinical trial was conducted to evaluate the efficacy of MQ for IPTp among HIV-infected women receiving CTX (NCT 00811421: Pan African Clinical Trials Registry PACTR 2010020001813440) . As part of this larger trial, a nested investigation of the pharmacokinetics of MQ and its effect on the blood levels of CTX was conducted in a sub-sample of HIV-infected pregnant women enrolled into the main trial at the site in Kisumu, Kenya.
The double-blinded, placebo-controlled study took place at the Siaya District Hospital, situated in an area of western Kenya with holo-endemic malaria transmission and a high prevalence of HIV. The main trial has been described in more detail elsewhere . Following clinical examination, women with a gestational age ≤28 weeks were included in the study, whereas IPTp was given only if the gestational age was greater than 13 weeks. The MQ arm received the first dose of IPTp (15 mg/kg MQ) under supervision along with a continued daily dose of CTX (800 mg sulfamethoxazole, 160 mg trimethoprim). Each MQ tablet contains 250 mg of mefloquine HCl. The number of MQ tablets administered to a woman was determined according to the maternal weight at the time of first IPTp administration (i.e., a woman weighing 60 kg received three-and-a-half MQ tablets). Women in the placebo arm received placebo MQ at the same schedule as for the MQ arm, as well as CTX. CTX was administered daily and a total of three doses of MQ or placebo were administered at least 1 month apart. HIV-infected pregnant women who met all the enrolment criteria for the main trial, and reported having taken CTX on a daily basis in the previous 7 days, were invited to participate in this nested study. Participants from the main study who verbally reported having taken CTX on a daily basis in the past week underwent a standard informed consent procedure at enrolment into the nested pharmacokinetic (PK) study. The institutional review boards of the Kenya Medical Research Institute (Nairobi, Kenya), the US Centers for Disease Control and Prevention (Atlanta, GA, USA) and the Hospital Clinic of Barcelona (Spain) approved the study protocol. All women who participated gave written informed consent.
A total of 124 HIV-infected pregnant women were selected for MQ, sulfamethoxazole (SMX) and trimethoprim (TMP) analysis. After disclosure of the MQ and placebo groups, 72 of 124 subjects had received MQ. The PK parameters for MQ were determined from this group. The subjects were randomly divided into three groups: Group A provided blood samples at two, 14 and 28 days, Group B provided samples at 4 h, 1 and 7 days, and Group C provided samples at 8 h, 3 and 21 days. On days 0, 1, 3, 7, 14, 21, and 28, blood samples were collected prior to the next dose of co-trimoxazole in order to obtain the minimal steady-state concentrations of SMX and TMP. All the subjects provided a sample at day 0 (pre-dose). Final number of samples collected per time point ranged from 13 to 22 with a median of 18. Sixteen samples per time point is enough to detect 25 % change (α = 0.05, β = 0.02), considering the estimated % coefficient of variation (% CV) for inter-individual MQ blood concentration to be 35 % (derived from previous laboratory experience performing MQ analyses) (MedCalc Statistical Software version 13.2.0 (MedCalc Software bvba, Ostend, Belgium). At day 7 following a second monthly dose of MQ, blood was collected for analysis to observe any accumulation.
Blood sample collection
At the appropriate time point, approximately 0.5 ml whole blood was collected by venipuncture. Three blood spots were prepared on Whatman No 1 filter paper by transferring 0.1 ml of whole blood using a positive displacement pipette. The spotted filter papers were air-dried, individually wrapped, labelled, and transferred to plastic bags containing a small amount of silica to prevent moisture accumulation. All dried blood spots were stored in a refrigerator (4 °C) until transported to CDC via travelling personnel. After delivery, samples were stored at −20 °C until analysis.
A modification of a high-performance liquid chromatographic (HPLC) method described by Bergqvist et al. was used to simultaneously measure TMP, SMX, and MQ in dried blood spots . TMP, SMX and MQ analytical standards were generously donated by WWARN (Worldwide Antimalarial Resistance Network). A 4.6 × 150 mm, 5 μ, C18 column (Supelco) coupled to a 2.1 × 10 mm, 3.5 μ, RP8 guard column (Symmetryshield) and a mobile phase consisting of 30 % acetonitrile and 70 % water containing 20 mM N,N-dimethyloctylamine adjusted to pH 2.3 with phosphoric acid was used to separate the components. The column temperature was set for 30 °C and the mobile phase flow rate set for 1 ml/min. The components were detected using a diode array detector with wavelength set at 280 and 220 nm. Drug extraction from dried blood spots was accomplished by combining a solid phase technique for sulfonamides  with liquid–liquid extraction for MQ . Samples were analysed in duplicate. The dried blood spots were cut into four sections and inserted into a polypropylene tube containing 100 ml of phenacetin (10 μg/ml in methanol) as an internal standard for SMX and TMP quantitation and 50 ml of the mefloquine derivative WR184806 (29 mg/ml in methanol) as an internal standard for MQ quantitation; 1.5 ml of sodium hydroxide (0.1 M) was added and the papers allowed to soak for 10 min. The tubes were rotated for 15 min followed by removal of the filter papers. A volume of 0.25 ml zinc sulfate (1 M) was added and the tubes rotated for 15 min followed by centrifugation for 10 min at 4000 rpm. The supernatant was added to prepped 100 mg C8 solid-phase extraction columns and eluted by vacuum. The column matrix was washed with 0.5 ml of water and the SMX and TMP eluted with 1 ml of acetone containing 2 % triethylamine. For the MQ extraction, 1.5 ml of pH 9 phosphate buffer was added to the pellet and sonicated for 10 min; 5 ml of methyl t-butyl ether was added and the tubes rotated for 10 min followed by centrifugation for 5 min at 2000 rpm. The organic phase layer was transferred to the appropriate tubes containing the acetone eluent. Extraction with methyl t-butyl ether was repeated and the organic phase combined with the previous extracts from the appropriate samples. The extract was evaporated to dryness with nitrogen, reconstituted in mobile phase and injected into the HPLC for analysis. The extraction method was not optimized for measuring blood levels of the major metabolites, carboxymefloquine and N-acetyl sulfadoxine, although these components were effectively separated by HPLC. Blood concentrations for each component were determined from a standard curve consisting of a series of spiked dried blood spots. Evaluation of the analysis method for ten standard curve runs showed the % coefficient of variation to be 11, 7 and 26 % for MQ (594 ng/ml), SMX (27.5 mg/ml) and TMP (1.8 mg/ml), respectively. The relatively high variation for TMP was a result of the low concentrations in blood which was approaching detection limits. The % accuracy was 4.2, 1.5 and 0.2 % for MQ, SMX and TMP, respectively. Some samples had large unidentified chromatographic peaks that interfered with the analytes, possibly resulting from other ingested medications. Therefore, blood concentration values for each time point were subjected to the Tukey Outlier Test  where values larger than the upper quartile plus three times the interquartile range were eliminated. Only one outlier, occurring at day 7 was eliminated from the MQ concentration–time curve. No more than two outliers per time point was eliminated from the TMP data. The remaining blood concentration values were then averaged for each time point and used for the pharmacokinetic analysis.
Characteristics of subjects upon enrolment
MQ arm (n = 72)
Placebo arm (n = 52)
Body weight (kg)
Comparison of pharmacokinetic parameters for mefloquine
Ramharter et al. (pers comm)
Desjardins et al. 
Schwartz et al. 
De Souza et al. 
Na Bangchang et al. 
Pregnant (P. falciparum)
Non-pregnant Females (P. falciparum)
Nosten et al. 
Drug interactions can occur as a result of competitive or non-competitive inhibition of the Cytochrome p450 enzyme. The Cytochrome p450 isoform, CYP3A4, has been implicated in MQ metabolism since the co-administration of ketoconazole, a potent inhibitor of CYP3A4 was shown to significantly increase plasma MQ levels in humans . Since SMX and TMP have negligible effects on the CYP3A4 isoform , it is expected that SMX and TMP will have little effect on MQ pharmacokinetics. Although, the results did not show any significant changes in MQ pharmacokinetics in the presence of steady-state levels of SMX and TMP, a significant reduction of SMX levels upon MQ administration was observed. A reduction of SMX levels has also been observed in HIV-infected individuals administered rifampin and has been attributed to enhanced SMX hepatic acetylation . MQ or its metabolite, carboxymefloquine may affect SMX metabolism similarly. The rapid reduction of SMX levels 4 h after MQ administration (Fig. 2) may be attributed to the presence of either MQ or its metabolite, carboxymefloquine. If MQ has a direct effect on SMX metabolism, SMX levels would be expected to rise after MQ begins its elimination phase at approximately 4 h. Although an unexplained elevation of SMX levels is seen at day 2, the lowest levels occur at day 7 followed by an exponential rise to MQ pre-dose levels at day 28. The rise in SMX levels at day 7 corresponds to the beginning of the elimination phase (tmax = 9 ± 3 days) for the carboxymefloquine metabolite . The rate of SMX increase was determined by fitting an exponential growth equation (y = aebx) to SMX concentrations from seven to 28 days. The growth constant (b) of 0.0015 h−1 is equal to a doubling time of 19 days. The half-life for carboxymefloquine of 21 days  corresponds to the doubling time of SMX of 19 days, suggesting that the presence of the carboxymefloquine metabolite may influence SMX metabolism. A recent study has shown that the major metabolite of MQ, carboxymefloquine induces the expression of drug metabolizing enzymes and transporters by activating the pregnane X receptor .
Limitations of this study include the lack of sufficient blood samples collected during the MQ absorption phase to obtain accurate tmax, Cmax, as well as the absorption rate constant (ka). Obtaining multiple blood samples in a short period of time required for absorption phase kinetics is difficult under the conditions encountered in developing countries. Drug metabolites were not quantified using the described analytical technique, therefore any associations with metabolite levels could not be made directly. Although no significant differences were seen for TMP between the MQ and placebo arm, low levels and high variability may have masked any changes. Over 95 % of the subjects in the study were taking an antiretroviral medication (mostly zidovudine, lamivudine, and nevirapine) concomitant with MQ and CTX. Possible interactions with these antiretrovirals cannot be ruled out.
This is the first study assessing the pharmacokinetic inter-relationship of MQ and CTX. In this study, prophylactic levels of CTX did not significantly alter MQ pharmacokinetics in HIV-infected pregnant women relative to reported parameters in pregnant women not receiving CTX. While exposure to MQ did not affect TMP levels, there is concern that the transient decline in SMX levels would result in an increase in hospital admissions from secondary bacterial infections. However, this was not the case. Results from the multi-site clinical trial from which this study is derived do not support this assertion . This implies that that the antimicrobial properties of MQ may have provided some protection against microbial infections .
MG conceived the study, participated in its design, performed the drug analysis, processed the data, performed the pharmacokinetic analysis and drafted the manuscript. KO collected data, processed laboratory samples, and participated in interpretation and write-up. AK conceived the study, collected and interpreted the data. LS conceived the study and interpreted the data. SK collected and interpreted data, participated in the write-up and was responsible for the oversight of laboratory work. PO collected and interpreted data and responsible for oversight. RG interpreted the data and participated in the write-up. CM interpreted the data and participated in the write-up. FK conceived the study, interpreted the data, and participated in the write-up. MD conceived the study, participated in its design and coordination and helped draft the manuscript. All authors read and approved the final manuscript.
The work presented in this paper was performed under KEMRI and CDC collaboration in western Kenya. We thank all the women who patiently participated in the study. We also thank the staff, Joab Middii, Mary Omwalo, Denis Omondi, and Arthur Juma Okumu for their assistance. We thank the Director of the Kenya Medical Research Institute (KEMRI) for his support. Funding was provided by the Malaria in Pregnancy Consortium. The findings and conclusions in this article do not necessarily reflect the views of the Centers for Disease Control and Prevention. The use of trade names is for identification only and does not imply endorsement by the Public Health Service or the US Department of Health and Human Services.
The authors declare that they have no competing interests.
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- Ter Kuile FO, Parise ME, Verhoeff FH, Udhayakumar V, Newman RD, Van Eijk AM, et al. The burden of co-infection with human immunodeficiency virus type 1 and malaria in pregnant women in sub-Saharan Africa. Am J Trop Med Hyg. 2004;71(suppl 2):41–54.PubMedGoogle Scholar
- WHO. Malaria in HIV/Aids patients. Geneva: World Health Organization. http://who.int/malaria/areas/high_risk_groups/hiv_aids_patients/en/index.html.
- Ward SA, Sevene EJ, Hastings IM, Nosten F, McGready R. Antimalarial drugs and pregnancy: safety, pharmacokinetics, and pharmacovigilance. Lancet Infect Dis. 2007;7:136–44.PubMedView ArticleGoogle Scholar
- Nosten F, McGready R, Mutabingwa T. Case management of malaria in pregnancy. Lancet Infect Dis. 2007;7:118–25.PubMedView ArticleGoogle Scholar
- Wilby K, Ensom M. Pharmacokinetics of antimalarials in pregnancy: a systematic review. Clin Pharmacokinet. 2011;50:705–23.PubMedView ArticleGoogle Scholar
- WHO. A strategic framework for malaria prevention and control during pregnancy in the African region. AFR/MAL/04/01. Brazzaville: World Health Organization Regional Office for Africa; 2004.Google Scholar
- Menendez C, D’Alessandro U, ter Kuile FO. Reducing the burden of malaria in pregnancy by preventive strategies. Lancet Infect Dis. 2007;7:126–35.PubMedView ArticleGoogle Scholar
- Crawley J, Hill J, Yartey J, Robalo M, Serufilira A, Ba-Nquz A, et al. From evidence to action? Challenges to policy change and programme delivery for malaria in pregnancy. Lancet Infect Dis. 2007;7:145–55.PubMedView ArticleGoogle Scholar
- Nosten F, Karbwang J, White N, Honeymoon, Na Bangchang K, Bunnag D, et al. Mefloquine antimalarial prophylaxis in pregnancy: dose finding and pharmacokinetic study. Br J Clin Pharmacol. 1990;30:79–85.PubMedPubMed CentralView ArticleGoogle Scholar
- Na Bangchang K, Davis T, Looareesuwan S, White N, Bunnag D, Karbwang J. Mefloquine pharmacokinetics in pregnant women with acute falciparum malaria. Trans R Soc Trop Med Hyg. 1994;88:321–3.Google Scholar
- Moore KH, Yuen GJ, Raasch RH, Eron JJ, Martin D, Mydlow PK, Hussey EK. Pharmacokinetics of lamivudine administered alone and with trimethoprim–sulfamethoxazole. Clin Pharmacol Ther. 1996;59:550–8.PubMedView ArticleGoogle Scholar
- Sturgill MG, Seibold JR, Boruchoff SE, Yeh KC, Haddix H, Deutsch P. Trimethoprim/sulfamethoxazole does not affect the steady-state disposition of indinavir. J Clin Pharmacol. 1999;19:1077–84.View ArticleGoogle Scholar
- Abel S, Russell D, Whitlock LA, Ridgway CE, Muirhead GJ. The effects of cotrimoxazole or tenofovir coadministration of the pharmacokinetics of maraviroc in healthy volunteers. Br J Clin Pharmacol. 2008;65:47–50.PubMedPubMed CentralView ArticleGoogle Scholar
- Canas E, Pachon J, Garcia-Pesquera F, Castillo JR, Viciana P, Cisneros JM, et al. Absence of effect of trimethoprim–sulfamethoxazole on pharmacokinetics of Zidovudine in patients infected with human immunodeficiency virus. Antimicrob Agents Chemother. 1996;40:230–3.PubMedPubMed CentralGoogle Scholar
- Ribera E, Pou L, Fernandez-Sola A, Campos F, Lopez RM, Ocana I, et al. Rifampin reduces concentrations of trimethoprim and sulfamethoxazole in serum of human immunodeficiency virus-infected patients. Antimicrob Agents Chemother. 2001;45:3238–41.PubMedPubMed CentralView ArticleGoogle Scholar
- ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT00811421.
- Gonzalez R, Desai M, Macete E, Ouma P, Kakolwa MA, Abdulla S, et al. Intermittent preventive treatment of malaria in pregnancy with mefloquine in HIV-infected women receiving cotrimoxazole prophylaxis: a multicenter randomized placebo-controlled trial. PLoS Med. 2014;11:e1001735.PubMedPubMed CentralView ArticleGoogle Scholar
- Bergqvist Y, Eckerbom S, Larsson N, Churchill F. High-performance liquid chromatographic separation and extraction investigation for the simultaneous determination of mefloquine and its carboxylic acid metabolite. J Chromatogr. 1988;427:295–305.PubMedView ArticleGoogle Scholar
- Green M, Mount D, Nettey H. High-performance liquid chromatographic assay for the simultaneous determination of sulfadoxine and pyrimethamine from whole blood dried onto filter paper. J Chromatogr. 2002;B767:159–62.Google Scholar
- Tukey JW. Some thoughts on clinical trials, especially problems of multiplicity. Science. 1977;198:679–84.PubMedView ArticleGoogle Scholar
- Desjardins RE, Pamplin CL, Von Bredow J, Barry KG, Canfield CJ. Kinetics of a new antimalarial, mefloquine. Clin Pharmacol Ther. 1979;26:372–9.PubMedView ArticleGoogle Scholar
- Mahmood I. Naïve pooled-data approach for pharmacokinetic studies in pediatrics with a very small sample size. Am J Ther. 2014;21:269–74.PubMedGoogle Scholar
- Schwartz DE, Eckert G, Hartmann D, Weber B, Richard-Lenoble D, Ekue JM, et al. Single dose kinetics of mefloquine in man. Chemotherapy. 1982;28:70–84.PubMedView ArticleGoogle Scholar
- Karbwang J, Back DJ, Bunnag D, Breckenridge AM. A comparison of the pharmacokinetics of mefloquine in healthy Thai volunteers and in Thai patients with falciparum malaria. Eur J Clin Pharmacol. 1988;35:677–80.PubMedView ArticleGoogle Scholar
- Looareesuwan S, White NJ, Warrell DA, Forgo I, Dubach UG, Ranalder UB, et al. Studies of mefloquine bioavailability and kinetics using a stable isotope technique: a comparison of Thai patients with falciparum malaria and healthy Caucasian volunteers. Br J Clin Pharmacol. 1987;24:37–42.PubMedPubMed CentralView ArticleGoogle Scholar
- DeSouza JM, Heizmann P, Schwartz DE. Single dose kinetics of mefloquine in Brazilian male subjects. Bull World Health Organ. 1987;65:353–6.Google Scholar
- Franssen G, Rouveix B, Lebras J, Bauchet J, Verdier F, Michon C, et al. Divided-dose kinetics of mefloquine in man. Br J Clin Pharmac. 1989;28:179–84.View ArticleGoogle Scholar
- Boudreau EF, Fleckenstein L, Pang LW, Childs GE, Schroeder AC, Ratnaratorn B, et al. Mefloquine kinetics in cured and recrudescent patients with acute falciparum malaria and in healthy volunteers. Clin Pharmacol Ther. 1990;48:399–409.PubMedView ArticleGoogle Scholar
- Weidekamm E, Rusing G, Caplain H, Sorgel F, Crevoisier C. Lack of bioequivalence of a generic mefloquine tablet with the standard product. Eur J Clin Pharmacol. 1998;54:615–9.PubMedView ArticleGoogle Scholar
- Kaplan SA, Weinfeld RE, Abruzzo CW, McFaden K, Jack ML, Weissman L. Pharmacokinetic profile of trimethoprim in man. J Infect Dis. 1973;128:S547–55.View ArticleGoogle Scholar
- Nowak A, Klimowicz A, Kadykow M. Distributioin of trimethoprim and sulphamethoxazole in blood during treatment with co-trimoxazole. Eur J Clin Pharmacol. 1985;29:231–4.PubMedView ArticleGoogle Scholar
- Kremers P, Duvivier J, Heusghem C. Pharmacokinetic studies of co-trimoxazole in man after single and repeated doses. J Clin Pharm. 1974;14:112–7.View ArticleGoogle Scholar
- Klepser M, Zhu Z, Nicolau DP, Banevicius MA, Belliveau PP, Ross JW, et al. Oral absorption of trimethoprim–sulfamethoxazole in patients with AIDS. Pharmacotherapy. 1996;16:656–62.PubMedGoogle Scholar
- Green MD, Van Eijk AM, Ter Kuile FO, Ayisi JG, Parise ME, Kager PA, et al. Pharmacokinetics of sulfadoxine–pyrimethamine in HIV-infected and uninfected pregnant women in Western Kenya. J Infect Dis. 2007;196:1403–8.PubMedView ArticleGoogle Scholar
- Ridtitid W, Wongnawa M, Mahatthanatrakul W, Raungsri N, Sunbhanich M. Ketoconazole increases plasma concentrations of antimalarial mefloquine in healthy human volunteers. J Clin Pharm Ther. 2005;30:285–90.PubMedView ArticleGoogle Scholar
- Wen X, Wang JS, Backman JT, Laitila J, Neuvonen PJ. Trimethoprim and sulfamethoxazole are selective inhibitors of CYP2C8 and CYP2C9, respectively. Drug Metab Dispos. 2002;30:631–5.Google Scholar
- Piedade R, Traub S, Bitter A, Nüssler AK, Gil JP, Schwab M, et al. Carboxymefloquine, the major metabolite of the antimalarial drug mefloquine, induces drug-metabolizing enzyme and transporter expression by activation of pregnane X receptor. Antimicrob Agents Chemother. 2015;59:96–104.PubMedPubMed CentralView ArticleGoogle Scholar
- Kunin CM, Ellis WY. Antimicrobial activities of mefloquine and a series of related compounds. Antimicrob Agents Chemother. 2000;44:848–52.PubMedPubMed CentralView ArticleGoogle Scholar
- Eatman FB, Maggio AC, Pocelinko R, Boxenbaum HG, Geitner KA, Glover W, et al. Blood and salivary concentrations of sulfamethoxazole and trimethoprim in man. J Pharmacokinet Biopharm. 1977;5:615–24.PubMedView ArticleGoogle Scholar