There is a worldwide upscale in mass drug administration (MDA) programs to control the morbidity caused by soil-transmitted helminths (STHs): Ascaris lumbricoides, Trichuris trichiura and hookworm. Although anthelminthic drugs which are used for MDA are supplied by two pharmaceutical companies through donation, there is a wide range of brands available on local markets for which the efficacy against STHs and quality remain poorly explored. In the present study, we evaluated the drug efficacy and quality of two albendazole brands (Bendex and Ovis) available on the local market in Ethiopia.
A randomized clinical trial was conducted according to the World Health Organization (WHO) guidelines to assess drug efficacy, by means of egg reduction rate (ERR), of Bendex and Ovis against STH infections in school children in Jimma, Ethiopia. In addition, the chemical and physicochemical quality of the drugs was assessed according to the United States and European Pharmacopoeia, encompassing mass uniformity of the tablets, amount of active compound and dissolution profile. Both drugs were highly efficacious against A. lumbricoides (>97%), but showed poor efficacy against T. trichiura (~20%). For hookworms, Ovis was significantly (p < 0.05) more efficacious compared to Bendex (98.1% vs. 88.7%). Assessment of the physicochemical quality of the drugs revealed a significant difference in dissolution profile, with Bendex having a slower dissolution than Ovis.
The study revealed that differences in efficacy between the two brands of albendazole (ABZ) tablets against hookworm are linked to the differences in the in-vitro drug release profile. Differences in uptake and metabolism of this benzimidazole drug among different helminth species may explain that this efficacy difference was only observed in hookworms and not in the two other species. The results of the present study underscore the importance of assessing the chemical and physicochemical quality of drugs before conducting efficacy assessment in any clinical trials to ensure appropriate therapeutic efficacy and to exclude poor drug quality as a factor of reduced drug efficacy other than anthelminthic resistance. Overall, this paper demonstrates that “all medicines are not created equal”.
Soil-transmitted helminths (STHs) infect millions of children worldwide. To fight STH, large-scale de-worming programs are implemented in which anthelmintic drugs (either albendazole (ABZ) or mebendazole (MEB)) are administered. However, there is a wide range of other brands, which are even more accessible, but for which the efficacy and quality remain poorly explored. We evaluated efficacy against STHs and quality of two ABZ brands commonly available on the local markets in Ethiopia (Bendex and Ovis). Both brands showed high efficacy against roundworm infections and poor efficacy against whipworms. However, for hookworm infections, Bendex was significantly less efficacious than Ovis. In terms of drug quality, a significant difference was observed in the dissolution profile, with Bendex having a significantly slower dissolution rate than Ovis. Since dissolution behavior is critical for a drug to be appropriately absorbed into the helminth (through host-blood and/or parasite-cuticle) and produce therapeutic efficacy, the poor dissolution of Bendex compared to Ovis can explain the observed difference in efficacy against hookworms. Our results emphasize the importance of periodically assessing of drug quality to ensure appropriate therapeutic efficacy and to exclude poor drug quality as a potential factor of reduced drug efficacy other than drug resistance.
Citation: Belew S, Getachew M, Suleman S, Mohammed T, Deti H, D'Hondt M, et al. (2015) Assessment of Efficacy and Quality of Two Albendazole Brands Commonly Used against Soil-Transmitted Helminth Infections in School Children in Jimma Town, Ethiopia. PLoS Negl Trop Dis 9(9): e0004057. https://doi.org/10.1371/journal.pntd.0004057
Editor: Maria Victoria Periago, Fundación Mundo Sano, ARGENTINA
Received: April 17, 2015; Accepted: August 14, 2015; Published: September 25, 2015
Copyright: © 2015 Belew et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: BL is a postdoctoral fellow of the Fund for Scientific Research-Flanders (Belgium) (F.W.O.-Vlaanderen, grant no. FWO12/PDO/099). BOF (Special Research Fund) is funding a PhD scholarship of SB in Gent University (Scholarship code 01W03714, Reference number DOZA/ILDDC/AM/0866b-2014). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Currently, there is a worldwide upscale in the implementation of programs to control and to eliminate a selection of 10 neglected tropical diseases [1, 2]. Among these, soil-transmitted helminthiasis causes the highest burden on public health. It is estimated that more than 1.4 billion people were infected with at least one of the four STH species: the roundworm Ascaris lumbricoides, the whipworm Trichuris trichiura and the two hookworm species Necator americanus and Ancylostoma duodenale, resulting in a global burden of approximately 5.2 million disability-adjusted life years (DALYs) (20% of the total number of DALYs attributable to neglected tropical diseases) [3, 4]. To control the morbidity caused by STH, mass drug administration (MDA) of a single oral dose of a benzimidazole anthelminthic drug (ABZ or MEB) is recommended in communities where the prevalence of any STH exceeds 20% .
To date, major pharmaceutical companies such as GlaxoSmithKline (ABZ, Zentel) and Johnson and Johnson (MEB, Vermox) are donating these medicines to WHO, which subsequently distribute these medicines to its recipient countries. In Ethiopia, the donated medicines are made available for the patients through government hospitals and health centers. The therapeutic efficacy of these products at the WHO-recommended dosages (i.e. single dose of 400 mg ABZ or 500 mg MEB) has recently been evaluated in two consecutive multinational trials [6, 7]. These trials showed that the therapeutic efficacy measured in terms of egg reduction rate (ERR), varied both between drugs and STH species: both drugs showing high efficacy against A. lumbricoides (> 98%) and poor efficacy against T. trichiura (~64%), and ABZ being more efficacious against hookworms compared to mebendazole (96% vs. 80%). In addition to these two donated brands, there is a wide range of other brands available on local markets of STH endemic countries, which are often more accessible to the local people, but for which the efficacy or quality remain poorly explored . The latter is particularly important in countries where resources are limited to monitor the quality of drugs, and hence in which prevalence of substandard, falsified or illegal drugs is substantial [9–14]. Although the quality of medicines has a direct influence on therapeutic efficacy, this remains poorly studied for benzimidazole anthelminthic drugs against STH infections. Therefore, we assessed both the efficacy and quality of two brands of ABZ commonly administered for the treatment of individual STHs in Ethiopia, namely Bendex and Ovis.
The study protocol was approved by the Ethical Committees of Jimma University (Ethiopia) (reference no RPGC/282/2014) and of the Faculty of Medicine, Ghent University (Belgium) (ref. no 2013/1114; B670201319330). The study is registered under clinicaltrial.gov identifier number NCT02420574 (https://clinicaltrials.gov/ct2/show/NCT02420574?term=NCT02420574&rank=1). The school authorities, teachers, parents, and the children were informed about the purpose and procedures of the study. The written consent form was prepared in two commonly used local languages (Afaan Oromo and Amharic) and handed over to the children’s parents/guardians after explaining the aim, confidentiality and entire procedure of the clinical trial. Only those children (i) who were willing to participate and (ii) whose parents or guardians signed the written informed consent form were included in the study. Moreover, an additional separate written informed consent form for children older than 12 years was prepared, read and handed over to them and their additional written informed consent obtained (S1 Checklist).
Origin of the drugs
Samples of the two ABZ brands (Bendex, India, CIPLA Ltd, batch no: x21253 and Ovis, Korea, DaeHWa Pharmaceuticals, batch no: 2020) with a label claim of 400 mg/tablet and expiry date of November 2015 were purchased from private community pharmacy in Jimma town, Ethiopia.
Assessment of therapeutic efficacy against STH infections in school children
Study site and study population.
The study was conducted in Jimma town, Ethiopia, which is located approximately 350 km southwest of the capital Addis Ababa. This study focused on school children (aged 5 to 18 years) from 2 out of the 24 primary schools that are found in Jimma Town. These schools were selected based on previous STH prevalence data [15, 16] and their involvement in previous drug efficacy trials [6, 7, 17]. At the time of this trial, these schools were not included in any MDA program.
The initial objective of this study was to assess the efficacy of ALB medicines against STH infections in school children. To this end, we applied the recently published WHO guidelines on the efficacy assessment of anthelminthic drugs against Schistosomiasis and STH to evaluate the efficacy of both brands . In this guideline, at least 50 infected subjects per STH species are required. We also evaluated the quality of both medicines. Hence, this survey was originally not designed to assess a difference in ERR between brands, but merely to verify whether drugs were satisfactory, doubtful or unsatisfactory. Hence, no a prior power calculation was performed, but the results were repeated together with the 95% CI and p-value (at significant level of 5%). In short, parents/guardians were informed about the aims and the procedures of the entire clinical trial. Based on this, school children were recruited on a voluntary basis and asked to provide a stool sample during a pre-intervention survey. Among these, infected children who fulfill the WHO criteria for efficacy trial were enrolled for intervention. For the initial sampling, the aim was to enroll at least 100 infected children (50 for each ABZ brand) for A. lumbricoides, T. trichiura and hookworm, separately. Subjects with multiple infections were subsequently randomized across the two ABZ brands, stratifying for mono, double and triple STH infections. The drugs were administered under the direct supervision of a clinical nurse. Fourteen days after drug administration, stool samples were again collected from the subjects. All stool samples were processed by the McMaster egg counting method . A tutorial on how to perform the McMaster egg counting method can be found at http://www.youtube.com/watch?v=UZ8tzswA3tc. Subjects who were unable to provide a stool sample at follow-up, or who were experiencing a severe intercurrent medical condition (any medical conditions other than parasitic infection) or had diarrhea at the time of the first sampling, were excluded from the study. The flowchart summarizing the number of subjects recruited, enrolled, lost at follow-up and included in the statistical analysis is presented in Fig 1, bearing in mind that individual children may have double infections.
Assessment of drug quality
The quality of the drugs was evaluated by investigating three efficacy-critical quality attributes: (i) the mass uniformity, (ii) the amount of the active compound, and (iii) the dissolution of the tablets.
ABZ USP reference standard (Greenfield Pharmaceuticals, batch number: 20070504), Sulfuric acid AR (reagent chemicals service Ltd, United Kingdom), ammonium phosphate monobasic (extra pure, Cisco Research laboratory Pvt. Ltd., India), hydrochloric acid (36% w/v, Fisher Chemicals, Germany), sodium hydroxide (BDH Laboratory supplies, England), HPLC grade methanol and acetonitrile (CARLO ERBA Reagents, England) and ultrapure HPLC water (18.2 MΩ cm resistivity) were used.
Twenty tablets of each brand were randomly selected and individually weighed with a calibrated balance (Metter Toledo, AL204-1C, Switzerland) with experimentally determined operating range of 94.63 mg to 200 g and accuracy of 0.006% . This mass uniformity between tablets of each brand was evaluated against the European pharmacopoeia specification .
Amount of active compound.
The assay of the active pharmaceutical ingredient (API) was performed by a validated reversed-phase method according to USP , using an Agilent 1260 HPLC system equipped with an Agilent ZORBAX SB-18 column (150 x 4.6 mm, 5 μm) and UV-VIS Diode Array Detector. The detection wavelength, column temperature, flow rate of the mobile phase and injection volume were set at 254 nm, 25°C, 1 ml/min and 20 μl, respectively. The isocratic mobile phase used was composed of methanol and 0.05 M phosphate buffer (pH 5.5) (60:40% v/v). The analytical method was validated according to International Conference on Harmonisation (ICH) Q2(R1) recommendation . The linearity of the method was evaluated around the target label claim concentration (analytical aliquot concentration of 200 μg/ml) ranging from 160 to 240 μg/ml ABZ. The regression line was assessed by determining the 95% confidence interval (95% CI) of slope and intercept parameters as well as by evaluating the residual plot. Repeatability precision was evaluated by injecting six replicates of 100% test concentration (200 μg/mL) and percent relative standard deviation (%RSD) of the measurements was calculated. The accuracy and range of the method was determined by spike experiments at five different concentrations corresponding to 80, 90, 100, 110 and 120% of the nominal analytical concentration (200 μg/ml).
System suitability was evaluated by (1) the symmetry factor (As) of the ABZ reference standard, calculated using the European Pharmacopoeia (Ph. Eur.) equation As = w0.05 / 2d, where, w0.05 is the width of the peak at one twentieth of the peak height and d is the distance between the perpendicular dropped from the peak maximum and the leading edge of the peak at one twentienth of the peak height; and (2) injection repeatability by injecting (6 times) the ABZ reference standard solution. The Ph.Eur. system suitability test (SST) specifications were considered, i.e. As maximally 1.5 and percentage relative standard deviation (%RSD) maximally 0.85 .
The dissolution of both brands was evaluated using a dissolution apparatus II (paddle) (RC-6D Tian Jin optical instruments, China) following United States Pharmacopoeia recommendation . The dissolution medium (900 mL 0.1 N HCl) was transferred to vessels of dissolution apparatus and the temperature and the spindle rotation speed were set to 37 ± 0.5°C and 50 rpm, respectively. Three tablets from each brand were randomly assigned to the six dissolution vessels and 10.0 ml samples were withdrawn at predetermined time points (0, 15, 30, 35, 40, 45 min) and replenished with an equal volume of fresh dissolution medium at the same temperature. The samples were immediately filtered using Whatman No. 1 filter paper and suitably diluted in 250 mL volumetric flask with 0.1 N sodium hydroxide. The absorbance of each sample was determined at 308 nm and 350 nm using a UV/Visible spectrophotometer (Aquarius, Cambridge, England) and the difference taken as absorbance value. A 0.1 N sodium hydroxide was used as the blank solution. The quantity in milligram (mg) of ABZ dissolved was calculated by the formula 22.5C(Au/As), where C is the concentration of ABZ reference standard (RS) in the standard solution (μg per mL) and Au and As are the absorbance differences, obtained at 308 nm and 350 nm, of the solution under test (Au) and the standard solution (As). This method was also validated according to ICH Q2(R1) recommendations, for linearity, precision and accuracy . In order to clarify one of the possible reasons to explain the different dissolution behavior, IR spectra of both tablets were recorded on a qualified FTIR spectrometer (Thermo Scientific, USA), using the KBr-disk methodology as described in the Ph. Eur. .
Assessment of drug efficacy.
Based on the obtained ERR results, the efficacy of the brands were classified as ‘satisfactory’, ‘doubtful’ and ‘reduced’. The criteria applied for this classification were suggested by WHO  and are summarized in Table 1. The 95% confidence intervals (95% CI) for age, sex ratio and FEC at baseline, and ERR were determined by bootstrap analysis (10,000 iterations). Permutation tests were performed to verify differences between both groups . These permutation tests consisted of 2 consecutive steps. First, the permutation distribution under the null hypothesis that in average there was no difference in age, sex ratio, and FEC at baseline, and ERR between two treatment arms was generated. To this end, all individuals of both arms were randomly re-assigned to one of the treatment arms (the number of individuals in each treatment arm remained unchanged). The new mean age, sex ratio, FEC and ERR for each of the two treatment arms was determined and the absolute value of the difference in age, sex ratio, FEC and ERR between treatment arms was calculated. Next, this procedure was repeated 10,000 times. The distribution of these 10,000 permutated age, sex ratio, FEC and ERR differences represented the permutation distribution when the null hypothesis is true. Second, the probability of finding a value as extreme as the absolute value of the observed difference in age, sex ratio, FEC and ERR between the two treatment arms in this permutation distribution was determined. The level of significance was set at p < 0.05.
Assessment of drug quality
The uniformity of mass between tablets of each brand was evaluated against Pharmacopoeial specification limit.
Amount of active compound.
The appropriateness of the model was assessed by determining the 95% confidence interval (95% CI) of slope and intercept parameters of regression line as well as by evaluating the residual plot. The amount of active compound of the two brands were evaluated against Pharmacopoeial specification limit.
Data of the dissolution profile of the two brands were compared using various mathematical models, t-test and model independent approaches (difference factor (f1), similarity factor (f2) and dissolution efficiency (DE)). KinetDS software program was used to determine dissolution efficiency (DE) or the area under a dissolution curve between defined time points and the best fit model for the dissolution profile of both brands. Measures of goodness of fit (Akaike Information Criterion (AIC) and determination coefficient (r2)) were used to determine the performance of dissolution models.
Assessment of drug efficacy
In total, 679 subjects were recruited of which 418 subjects were enrolled and randomized across the two brands of ABZ (nBendex = nOvis = 209). T. trichiura was the most prevalent (69.4%), followed by A. lumbricoides (53.6%). Hookworm infections were found in 28.2% of the subjects. In total 388 subjects completed the trial (nBendex = 197; nOvis = 191), resulting in a compliance rate of more than 90%. There was no significant difference in mean age (Bendex: 10.3 years vs. Ovis: 10.3 years, p = 1.00), sex ratio (Bendex: 1.07 vs. Ovis: 0.87, p = 1.00) and mean fecal egg count (FEC) (A. lumbricoides: Bendex: 8,706 egg per gram of feces (EPG) vs. Ovis: 7,935, p = 0.69; T. trichiura: Bendex: 909 EPG vs. Ovis: 769, p = 0.45; hookworm: Bendex: 355 EPG vs. Ovis: 335, p = 0.79) between the two arms at baseline. Both brands showed high efficacy against A. lumbricoides (Bendex: 98.7% vs. Ovis: 97.8%, p = 0.64), and poor efficacy against T. trichiura (Bendex: 24.4% vs. Ovis: 20.4%, p = 0.81). For hookworm infections, Ovis was more efficacious than Bendex, though the difference was marginally significant (Bendex: 88.7% vs. Ovis: 98.1%, p = 0.05). Based on the WHO criteria to classify the efficacy of anthelminthic drugs (Table 1), both brands had satisfactory and reduced efficacy against A. lumbricoides and T. trichiura, respectively. For hookworms, Ovis had a satisfactory efficacy, whereas Bendex had a doubtful efficacy. A pairwise comparison of baseline parameters and drug efficacy between Bendex and Ovis are presented in S1 Table.
Assessment of drug quality
Amount of active compound.
Method validation results indicated the fitness-for-use of the applied HPLC method. The 95% CI for the regression slope equaled 20.47 (95% CI: 20.14 to 20.80) and y-intercept equaled 9.99 (95% CI: -57.44 to 77.41) together with r2 value of 0.999 and ANOVA F-value of 17,551 proved a strong positive linear relationship. In addition, random pattern of the residual plot showed a good fit of the linear model to the data. The %RSD (0.26) for repeatability of the method was within the specification limit (%RSD ≤ 0.85). The results of percent recovery (mean % ± %RSD = 99.59 ± 0.57% to 100.42 ± 0.11%) were within acceptable range. The comparative assay results of the two brands of albendazole tablets are presented in Table 2: no significant difference at 95% CI (p ≥ 0.05) was found. Both brands were found to be complying with the acceptance criteria for assay of ABZ tablets  i.e. 90–110% label claim.
The applied method was linear over concentrations ranging from 5 to 15 μg/ml of ABZ. The slope equaled 0.05 (95% CI: 0.04 to 0.05) and intercept equaled 0.02 (95% CI: -0.001 to 0.023) showed linear association between the UV-signal and concentration. In addition, the residual plot indicated a good fit of linear regression. The %RSD for repeatability of the method was 0.01%. The ABZ recovery (mean % ± %RSD) of this method ranged from 98.64 ± 0.00% to 103.18 ± 0.0.01%. The comparative in-vitro dissolution results of the two brands of ABZ tablets are presented in Fig 2.
A single-point comparison (amount of dissolved active pharmaceutical ingredient (Q) in 30 minutes) of the two brands of ABZ tablets indicated that Bendex released 20.1%, while Ovis released 84.9%. While Ovis complied with the acceptance criteria of United States Pharmacopoeia (USP) monograph, Bendex failed . The release profile between Bendex and Ovis was significantly (p = 0.002) different, as quantitatively expressed by the values of similarity factor (f2) and difference factor (f1) between the two brands being 11 and 74, respectively. The dissolution efficiency (DE) of Bendex (15.83) was lower than the corresponding value observed for Ovis (63.48). The infra-red (IR) spectra of Bendex and Ovis are presented in Figs 3 and 4.
IR spectra of both brands showed no significant difference between the two brands, suggesting the similarity in solid state polymorphic form of ABZ in both brands. The IR spectrum of the major excipient of Ovis (i.e. anhydrous dibasic calcium phosphate) did not interfere with the ABZ spectrum, while the excipients with interfering IR spectrum (i.e. sodium lauryl sulfate: 2957 and 2918 cm-1 and magnesium stearate: 2918 cm-1) were only present at much lower concentrations than ABZ in the Ovis tablet, hence neglecting their IR interference. Finally, the release kinetics of ABZ from both brands was evaluated using mathematical modeling. The results of measures of goodness of fit (i.e. AIC and r2) for different dissolution models are presented in S2 Table. The model that best fitted the dissolution data of both brands was Weibull with lag time: the fact that both brands best fitted the data is indicative for a similar release mechanism of albendazole from the tablets.
Assessing the quality and in-vivo efficacy differences between different brands of ABZ tablets are very critical to avoid indiscriminate use of different brands that could influence intended therapeutic outcomes. In the present study, we evaluated comparative in-vivo efficacy and in-vitro quality of two commonly available brands of ABZ tablets (Bendex and Ovis) that are used to treat STH infection.
The in-vivo efficacy results of two brands of ABZ against A. lumbricoides and T. trichiura determined in terms of ERR, suggest the susceptibility difference between the two STHs. Therapeutic efficacy of antihelmnthics can be influenced by various factors such as infection intensity and susceptibility of parasites. Thus the reduced efficacy of both brands against T. trichiura observed in the present study could be due to high level of infection intensity  and/or genetic modification of beta-tubulin gene [26, 27]. Since concentration of API at the target site of the parasites could be low due to metabolism and/or limited absorption of the drug by the parasite [28, 29], the reduced efficacy of both brands against T. trichiura might also be associated with the pharmacokinetics of ABZ in the parasite. The reduced efficacy of the two brands against T. trichiura observed in the present study is comparable to the results reported in the previous studies [6, 17]. The present finding, i.e. high prevalence of T. trichiura among other STHs in the study area together with the reduced efficacy results in ERR observed for single dose of ABZ 400 mg tablets, is supported by various literature findings [30–33]. This emphasizes the urgent need for alternative drugs and/or development of novel anthelmintic drugs to tackle this efficacy problem.
Medicines quality is a critical factor that could affect efficacy of drugs against parasites  and for biopharmaceutical classification system (BCS) class II  drugs like ABZ that have low solubility and high permeability, dissolution is the rate-limiting step for drug absorption. Hence, in-vivo/in-vitro correlation between blood concentration profile and dissolution profile may be expected. Since the bioavailability of ABZ to the host is very low and also shows variability between individuals , a decreased dissolution could significantly worsen bioavailability, which in turn diminishes in-vivo efficacy of both the parent drug and therapeutically active metabolite (ABZ sulphoxide). Moreover, the capacity of anthelminthics to dissolve appropriately is an essential characteristic that allows proper drug uptake by the parasites and therefore assures the appropriate drug efficacy. Therefore, the four times decreased dissolution of Bendex compared to Ovis (Fig 2) which could influence both local and systemic concentration is a plausible explanation for the efficacy difference between the two brands against hookworms, which are blood sucking parasites. Previous studies already indicated the differences in uptake and metabolism of benzimidazole drugs among different helminth species [28, 29], which may explain that the efficacy difference between the two brands was only observed against hookworms.
Though mass uniformity and content of API per tablet are critical quality attributes that could influence efficacy, comparable quality of both brands with respect to mass uniformity and ABZ content observed in the present study (Table 2) explain the efficacy difference between the two brands against hookworms is not associated with mass uniformity and content of API.
Considering a single point dissolution specification for ABZ tablets as described in the USP, i.e. Q ≥ 80% dissolved in 30 min , there is a statistically significant (p ≤ 0.05) difference observed between Bendex (Q = 20%) and Ovis (Q = 85%) (Fig 2). Also, the area under the dissolution curve between defined time points (0, 15, 30, 45 min) or DE quantifies the poor in-vitro dissolution of Bendex. While Ovis thus complied to the USP dissolution specifications, Bendex on the contrary did not. Although an undesirable polymorphic solid state of albendazole could be one of the reasons for the difference in dissolution behavior of API [37–39], the IR spectra (Figs 3 and 4) of Bendex and Ovis showed no significant difference between the two brands. The absence of significant observed shifts in IR-absorption indicates the similarity in polymorphic form of ABZ in both brands. Thus, the significant difference in dissolution observed between the two brands could not be associated with different polymorphic forms of ABZ. Whatever the reason of dissolution difference is, e.g. excipient and processing manufacturing conditions and stability, the poor dissolution behavior of Bendex observed in the present study is in accordance with the previous reports in which 41 samples out of 72 samples of solid oral dosage forms including ABZ tablets, different generic formulations of albendazole tablets and carbamazepine immediate-release products did not comply with the established acceptance criteria [40–42]. In general, it is important to note that quality of medicines could be one of the factors influencing outcomes of clinical trials. For instance, literature indicates the association of poor quality of locally manufactured antimalarial drugs: Sulfadoxine-Pyrimethamine with clinical failure of malaria treatment in Pakistan . Therefore, the results of the present study and a recent report by Newton and his colleagues  point to the requirement of guidelines for quality assurance of medicines used in clinical trials. Subjects lost at follow-up per STH species were the limitations of this study.
In conclusion, this study demonstrated that the two investigated brands of ABZ tablets are efficacious against A. lumbricoides and hookworm while both brands had reduced efficacy against T. trichiura. However, there was a significant difference between the two brands of ABZ against hookworm. While both brands showed comparable tablet mass uniformity and albendazole content, the in-vitro dissolution release profile between the two brands was significantly different, explaining the clinical efficacy difference observed. The results of the present study underscore the importance of assessing the chemical and physicochemical quality of drugs before conducting efficacy assessment in clinical trials to ensure appropriate therapeutic efficacy and to exclude poor drug quality as a factor of reduced drug efficacy other than anthelminthic resistance. Our in-vivo efficacy study clearly indicates the importance of appropriate quality medicines.
S1 Table. A pairwise comparison of baseline parameters and drug efficacy between Bendex and Ovis.
The authors are grateful to Food, Medicine and Health Care Administration and Control Authority (FMHACA) of Ethiopia for kindly donation of ABZ reference standard. Additionally, we would like to thank the staff of the Laboratory of Drug Quality of Jimma University (Markos Duguma, Henok Teshome, and Yimer Mekonnen) and the Neglected Tropical Disease (NTD) Laboratory of Jimma University (Bizuwarek Sharew, Yesufi Seid and Yerosa Dinsa) for their technical assistance. We acknowledge one of the reviewers for his/her George Orwell's inspiring quote 'All animals are equal, but some are more equal than others (from: Animal Farm)’, which was paraphrased in this manuscript as “all medicines are not created equal”. Finally, we would like to acknowledge the director, teachers, parents/guardians of the children of the two schools for their unfailing co-operation during the study.
Conceived and designed the experiments: BDS MD EW LD JV BL ZM SS MG SB. Performed the experiments: SB MG BL SS ZM MD TM HD. Analyzed the data: BDS BL MG LD SB ZM BL SS HD MD EW JV. Contributed reagents/materials/analysis tools: TM ZM SS BDS MD EW JV. Wrote the paper: MG SB BDS BL SS TM HD MD EW LD ZM JV.
- 1. World Health Organization. Soil-Transmitted Helminthiases: Eliminating soil-transmitted helminthiasis as a public health problem in children: Progress report 2001–2010 and strategic plan 2011–2020. Geneva: World Health organization, 2012. Available: http://whqlibdoc.who.int/publications/2012/9789241503129_eng.pdf.
- 2. Uniting to combat neglected tropical diseases: A conversation on progress, 2014. Available: http://unitingtocombatntds.org/event/2014-04-02/uniting-combat-ntds-conversation-progress.
- 3. Murray CJ, Vos T, Lozano R, Naghavi M, Flaxman AD, Michaud C, et al. Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990–2010: a systematic analysis for the global burden of disease study 2010. Lancet. 2012;380: 2197–2223. pmid:23245608
- 4. Pullan RL, Smith JL, Jasrasaria R, Brooker SJ. Global numbers of infection and disease burden of soil transmitted helminth infections in 2010. Parasit Vectors. 2014;7: 37. pmid:24447578
- 5. World Health Organization. Assessing the efficacy of anthelminthic drugs against schistosomiasis and soil-transmitted helminthiasis. Department of control of neglected tropical disease, preventive chemotherapy and transmission control. Geneva: World Health Organization, 2013. 1–39. Available: http://apps.who.int.
- 6. Vercruysse J, Behnke JM, Albonico M, Ame SM, Angebault C, Bethony JM, et al. Assessment of the anthelmintic efficacy of albendazole in school children in seven countries where soil-transmitted helminths are endemic. PLoS Negl Trop Dis. 2011;5: e948. pmid:21468309
- 7. Levecke B, Montresor A, Albonico M, Ame SM, Behnke JM, Bethony JM, et al. Assessment of anthelmintic efficacy of mebendazole in school children in six countries where soil-transmitted helminths are endemic. PLoS Negl Trop Dis. 2014;8: e3204. pmid:25299391
- 8. Legesse M, Erko B, Medhin G. Comparative efficacy of albendazole and three brands of mebendazole in the treatment of ascariasis and trichuriasis. East Afr Med J. 2004;81: 134–338. pmid:15293971
- 9. Monteiro AM, Wanyangu SW, Kariuki DP, Bain R, Jackson F, McKellar QA. Pharmaceutical quality of anthelmintics sold in Kenya. Vet Rec. 1998;142: 396–398. pmid:9586132
- 10. Surendran A. World agencies try to stem flood of fake drugs. Nat Med. 2004;10: 111.
- 11. Kelesidis T, Kelesidis I, Rafailidis PI, Falagas ME. Counterfeit or substandard antimicrobial drugs: a review of the scientific evidence. J Antimicrob Chemother. 2007;60: 214–236. pmid:17550892
- 12. Bersissa K, Adugna T, Ajebu N. Comparative efficacy of seven brands of albendazole against naturally acquired gastrointestinal nematodes in sheep in Hawassa, southern Ethiopia. Turk J Vet Anim Sci. 2010;34: 417–425.
- 13. Stephanie TG, Emmanuel NN. Quality control evaluation of brands of mebendazole 100 mg tablets on the illegitimate pharmacy outlets. Int J Pharm Pharm Sci. 2014;6: 355–357.
- 14. Suleman S, Zeleke G, Deti H, Mekonnen Z, Duchateau L, Levecke B, et al. Quality of medicines commonly used in the treatment of soil transmitted helminths and giardia in Ethiopia: a Nationwide survey. PLoS Negl Trop Dis. 2014;8: e3345. pmid:25473966
- 15. Mekonnen Z, Meka S, Ayana M, Bogers J, Vercruysse J, Levecke B. Comparison of individual and pooled stool samples for the assessment of soil-transmitted helminth infection intensity and drug efficacy. PLoS Negl Trop Dis. 2013a;7: e2189.
- 16. Dana D, Mekonnen Z, Emana D, Ayana M, Getachew M, Workneh N, et al. Prevalence and intensity of soil-transmitted helminth infections among pre-school age children in 12 kindergartens in Jimma town, southwest Ethiopia. Trans R Soc Trop Med Hyg. 2014;108: 673–740.
- 17. Mekonnen Z, Levecke B, Boulet G, Bogers JP, Vercruysse J. Efficacy of different albendazole and mebendazole regimens against high-intensity Trichuris trichiura infections in school children, Jimma, Ethiopia. Pathog Glob Health. 2013b;107: 207–209.
- 18. Levecke B, Behnke JM, Ajjampur SS, Albonico M, Ame SM, Charlier J, et al. A comparison of the sensitivity and fecal egg counts of the McMaster egg counting and Kato-Katz thick smear methods for soil-transmitted helminths. PLoS Negl Trop Dis. 2011;5: e1201. pmid:21695104
- 19. United States Pharmacopeia, USP 37/NF 32. General Chapters: Balances. The United States Pharmacopoeial Convention, 12601 Twinbrook Parkway, Rockville, MD; USA; 2014. pp. 52.
- 20. Ph. Eur. European Pharmacopoeia, 8th ed. Chapter 2.9.5. Uniformity of mass of single dose preparations. European Directorate for Quality of Medicines and Health care. Strasbourg, France; 2014. pp. 297–298.
- 21. United States Pharmacopeia, USP 37/NF 32. USP monographs: Albendazole tablets. The United States Pharmacopoeial Convention, 12601 Twinbrook Parkway, Rockville, MD; USA; 2014. pp. 1626–1627.
- 22. ICH Harmonized Tripartite Guideline. International conference on harmonization of technical requirements for registration of pharmaceuticals for human use: Validation of analytical procedures: text and methodology Q2(R1), 2005. Available: http://www.ich.org.
- 23. Ph. Eur. European Pharmacopoeia, 8th ed. Chapter 2.2.46. Chromatographic separation techniques. European Directorate for Quality of Medicines and Health care. Strasbourg, France; 2014. pp. 72–79.
- 24. Ph. Eur. European Pharmacopoeia, 8th ed. Chapter 2.2.24. Absorption spectrophotometery, Infrared. European Directorate for Quality of Medicines and Health care. Strasbourg, France; 2014. pp. 38–40.
- 25. Hesterberg T, Moore DS, Monaghan S, Clipson A, Epstein R, Craig BA. Bootstrap Methods and Permutation Tests. In: Moore DS, Monaghan S, Clipson A, Epstein R, Craig BA (eds.) Introduction to the Practice of Statistics. 7th ed. WH Freeman, New York; 2010. pp. 355–415.
- 26. Ghisi M, Kaminsky R, Maser P. Phenotyping and genotyping of Haemonchus contortus isolates reveals a new putative candidate mutation for benzimidazole resistance in nematodes. Vet Parasitol. 2007;144: 313–320. pmid:17101226
- 27. Diawara A, Drake LJ, Suswillo RR, Kihara J, Bundy DA, Scott ME, et al. Assays to detect β-Tubulin codon 200 polymorphism in Trichuris trichiura and Ascaris lumbricoides. PLoS Negl Trop Dis. 2009;3: e397. pmid:19308251
- 28. Solana HD, Rodriguez JA, Lanusse CE. Comparative metabolism of albendazole sulfoxide by different helminth parasites. Parasitol Res. 2001;87: 275–280. pmid:11355675
- 29. Hansen TV, Friis C, Nejsum P, Olsen A, Thamsborg SM. Uptake of benzimidazoles by Trichuris suis in-vivo in pigs. Int J Parasitol Drugs Drug Resist. 2014;4: 112–117. pmid:25057460
- 30. Serkadis D, Amare W, Nejat J, Zeleke M. Soil transmitted helminths and associated factors among school children in government and private primary school in Jimma town, southwest Ethiopia. Ethiop J Health Sci. 2013;23: 237–244. pmid:24307823
- 31. Keiser J, Utzinger J. Efficacy of current drugs against soil transmitted helminth infections. JAMA. 2008;299: 1937–1948. pmid:18430913
- 32. Bennett A, Guyatt H. Reducing intestinal nematode infection efficacy of albendazole and mebendazole. Parasitol Today. 2000;16: 71–74. pmid:10652492
- 33. Benjamin S, Said MA, Shaali MA, Isaac IB, Rainer A, Jorg H et al. Efficacy and safety of albendazole plus ivermectin, albendazole plus mebendazole, albendazole plus oxantel pamoate, and mebendazole alone against Trichuris trichiura and concomitant soil-transmitted helminth infections: a four-arm, randomised controlled trial. Lancet Infect Dis. 2015;15: 15.
- 34. Albonico M. Methods to sustain drug efficacy in helminth control programmes. Acta Trop. 2003;86: 233–242. pmid:12745140
- 35. Amidon GL., Lennernäs H, Shah VP, Crison JR. A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharmaceut Res. 1995;12: 413–420.
- 36. Marriner SE, Morris DL, Dickson B, Bogan JA. Pharmacokinetics of albendazole in man. Eur J Clin Pharmacol. 1986;30: 705–708. pmid:3770064
- 37. Zhang GG, Law D, Schmitt EA, Qiu Y. Phase transformation considerations during process development and manufacture of solid oral dosage forms. Adv Drug Deliv Rev. 2004;56: 371–390. pmid:14962587
- 38. Pranzo MB, Cruickshank D, Coruzzi M, Caira MR, Bettini R. Enantio-tropically related albendazole polymorphs. J Pharm Sci. 2010;99: 3731–3742. pmid:20112428
- 39. Vippagunta SR, Brittain HG, Grant DJ. Crystalline solids. Adv Drug Del Rev. 2001;48: 3–26.
- 40. World Health Organization. World Health Organization Drug Information. WHO. 2011;28: 223–224. Available: http://www.who.int/medicines/publications/druginformation/en/.shsn
- 41. Galia E, Horton J, Dressman JB. Albendazole Generics: A comparative in vitro study. Pharmaceut Res. 1999;16; 1871–1875.
- 42. Jose RM, Dulce KS, Marcela H, Alma RC, Adriana MD. Comparative in vitro dissolution study of carbamazepine immediate-release products using the USP paddles method and the flow-through cell system. Saudi Pharm J. 2014;22: 141–147. pmid:24648826
- 43. Leslie T, Kaur H, Mohammed N, Kolaczinski K, Rosalynn LO, Rowland M. Epidemic of Plasmodium falciparum malaria involving substandard antimalarial drugs, Pakistan, 2003. Emerg Infect Dis. 2009;15: 1753–1759. pmid:19891862
- 44. Newton PN, Schellenberg D, Elizabeth AA, Ravinetto R, Michael DG, Feiko OT et al. Quality assurance of drugs used in clinical trials: proposal for adapting guidelines. BMJ. 2015;350.