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Print version ISSN 1984-8250
Braz. J. Pharm. Sci. vol.47 no.3 São Paulo July/Sept. 2011
Flávia Dias Marques-MarinhoI, *; José Carlos da Costa ZanonII; Emilia SakuraiIII; Ilka Afonso ReisIII; Angélica Alves LimaIV; Cristina Duarte Vianna-SoaresI
IDepartment of Pharmaceutical Products, Faculty of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, MG
IIOuro Cordis Clinic, Santa Casa Hospital, Ouro Preto, MG
IIIDepartment of Statistics, ICEx, Federal University of Minas Gerais
IVDepartment of Clinical Analyses, Pharmacy School, Federal University of Ouro Preto, Ouro Preto, MG
Simvastatin is commercially available as tablets and compounded capsules in Brazil. Very few reports regarding these capsules' quality, and consequently their efficacy, are available. The pharmaceutical quality of 30 batches of 20 mg simvastatin capsules from the market was evaluated by weight determination, content uniformity, disintegration (Brazilian Pharmacopeia), assay and dissolution test (USP32 tablet monograph). A HPLC method was developed for assay, content uniformity and dissolution test, and specifications were also established. Out of the 30 batches evaluated, 29 showed capsule disintegration within 45 min and individual weight variation was within ±10% or ±7.5% relative to average weight, for < or > 300 mg, respectively. Only 27 batches met dissolution test criteria with values >80% of the labeled amount in 45 min; 21 batches showed simvastatin content between 90.0-110.0% of the labeled amount and 19 batches had at least 9 out of 10 capsules with content uniformity values between 85.0-115.0% of the labeled amount with RSD<6.0%. Only 14 of all (30) batches fully met pharmacopeial quality standards. The establishment of test conditions and specification parameters for simvastatin capsules showed that there are relevant pharmacopeial quality differences between batches compounded by different pharmacies. For 53.33% of the tested products hypercholesterolemic treatment efficacy may be compromised.
Uniterms: Compounded simvastatin capsules. Quality control. RP-HPLC.
No Brasil, a sinvastatina está comercialmente disponível na forma de comprimidos e cápsulas manipuladas. Poucos relatos estão disponíveis sobre a qualidade e, consequentemente, a eficácia dessas cápsulas. A qualidade de 30 lotes de sinvastatina 20 mg cápsulas do mercado foi avaliada através da determinação de peso, uniformidade de conteúdo, desintegração (Farmacopéia Brasileira), doseamento e teste de dissolução (monografia comprimidos USP32). Método por CLAE foi desenvolvido para o doseamento, uniformidade de conteúdo e teste de dissolução; além disso, especificações foram estabelecidas. Dos 30 lotes avaliados, 29 apresentaram desintegração da cápsula até 45 min e a variação do peso individual foi ± 10% ou ± 7,5% em relação ao peso médio, se < ou > 300 mg, respectivamente. Apenas 27 lotes preencheram os critérios do teste de dissolução com valores > 80% da quantidade rotulada, em 45 min, 21 lotes apresentaram conteúdo de sinvastatina entre 90,0-110,0% do valor rotulado e 19 lotes apresentaram pelo menos 9 em 10 cápsulas, com valores de uniformidade de conteúdo entre 85,0 -115,0% da quantidade rotulada com RSD < 6,0%. Apenas 14 de todos os lotes (30) atenderam completamente os padrões de qualidade farmacopéicos. O estabelecimento das condições para os testes e de especificações para os parâmetros das cápsulas de sinvastatina mostrou que houve diferenças relevantes na qualidade farmacopeica entre os lotes das cápsulas manipuladas por distintas farmácias. A eficácia do tratamento hipercolesterolêmico poderia estar comprometida para 53,33% dos produtos testados.
Unitermos: Sinvastatina. Cápsulas manipuladas. Controle de qualidade. FR-CLAE.
Simvastatin (SIM, Figure 1) is a lipid lowering agent widely used worldwide for the treatment of hypercholesterolemia and for reducing morbidity and mortality associated with chronic heart disease (The 4S, 1994). It is commercially available in tablet and capsule dosage forms. SIM capsules are manufactured in Brazil by compounding pharmacies.
The pharmaceutical sector reached its most dominant in the late 1980s when it became the focus of attention from the regulatory agencies (Bertollo, 2008). The creation of the National Sanitary Surveillance Agency/ANVISA, the Brazilian regulatory authority, led to greater concern over health and safety of products, health services, production supervision and drug sales (Brasil, 1999). In 2000, ANVISA published its first resolution act, RDC 33, aimed at achieving harmonization in the compounding pharmacies sector (Brasil, 2000). It became mandatory to evaluate the compounded products by the pharmacies with respect to their physico-chemical quality and different characteristics. The pharmacies had to adjust to this requirement in order to remain in the market, or else shut down. Only six years later, RDC 33 resolutions was replaced by the more comprehensive RDC 214 (Brasil, 2006). Amid much controversy over the latter, another regulation RDC 67 was subsequently published in 2007 (Brasil, 2007) and later updated with the current RDC 87 amendment in 2008 (Brasil, 2008). In this scenario, ANVISA quality requirements for products and services offered by compounding pharmacies increased upon each new RDC release, leading to the commercial survival only of those businesses who could adapt and comply. Standardized procedures, process monitoring, quality management, employee training and more rigorous quality control numbered among the requirements. A high investment in equipment, personnel training and hiring of outsourced services was necessary. Not all pharmacies could afford to meet all the demands to incorporate changes. Nevertheless, the importance of these requirements to share professional responsibility and ensure greater health safety for patients was acknowledged.
For the last ten years compounding pharmacies have been governed by specific legislation, although many doubts about product quality, safety and efficacy still remain. Quality control is hampered by the absence of specific monographs for compounded products, leading to a lack of standardization in quality evaluation by accredited analysis laboratories for health, as well as, by ANVISA (Brasil, 1999a). Despite the prevailing limitations in the compounding pharmaceutical field, the number of new pharmacies has increased in recent years, according to ANVISA and Compounding Pharmacists National Association/ANFARMAG data (ANVISA, 2005). Today, the importance of compounding pharmacies in the communities is incontestable. Compounded capsules can be dose personalized, less expensive than industrialized tablets, and economically more attractive for the population. In view of the social importance of the sector, the quality of SIM compounded capsules was evaluated in the present study given that it can directly influence the safety and efficacy of products.
MATERIAL AND METHODS
Simvastatin USP reference standard (RS, lot I0D382, 99.4% purity label claim, United States Pharmacopeia, Rockville, MD, USA), methanol HPLC grade (Tedia, Fairfield, OH, USA), phosphoric acid 85% (Merck, Darmstadt, Germany), sodium dodecyl sulphate (SDS; Pharmacopéia Ativos Magistrais, Barueri, SP, Brazil), sodium hydroxide (J.T. Baker, Phillipsburg, NJ, USA) and monobasic sodium phosphate (Vetec, Rio de Janeiro, RJ, Brazil) were used as received. Distilled or ultrapurified water (Milli-Q-Plus, Millipore, Bedford, MA, USA) was used when necessary.
Simvastatin 20 mg capsule batches were randomly acquired (April to July, 2009) from thirty compounding pharmacies in regard to site location in different regions of Belo Horizonte, southeast of Brazil. Six batches were donated and twenty four were purchased in the market. During the study, the compounded capsules were stored according to labeled instructions and when not specified were stored in a dry and fresh place at ambient temperature. Batch characteristics (color and size) and capsule unit price are described in Table I.
All capsules batches were submitted to weight determination, disintegration, content uniformity assessments and evaluated according to Brazilian Pharmacopeia general methods (Farmacopéia Brasileira, 1988, 1996). For weight determination, twenty units of each batch were individually weighed on an analytical microbalance (BP210D, Sartorius, Edgewood, NY, USA). The average weight (AW) was calculated along with individual capsule variation relative to AW. Specified individual variation could be less than ±10% or ±7.5% for AW < 300 mg or AW > 300 mg, respectively. If two or more units failed to meet the limits, the capsule (n=20) contents were removed and their weight was determined by mass difference. A maximum of two units outside the original range was tolerated, but their variation had to be less than double the specified limits. Disintegration time was determined using six units from each batch in an Erweka disintegrator (ZT3, Heusenstamm, Germany) equipped with chronometer and thermostatic bath at 37±1°C. The disintegration time limit for all capsules to completely disintegrate was 45 min. Content uniformity was performed on ten units from each batch. SIM was individually assayed by developed HPLC method after dilution in a 50 mL volumetric flask and successive dilution in methanol until SIM 40 μg/mL. Acceptance criteria were no more than one unit outside the specified limit of 85.0%-115.0% of the labeled amount (LA). However, the individual value had to fall within 75.0-125.0% LA and the relative standard deviation (RSD) had to be less than or equal to 6.0%. For assay and dissolution test conditions, the USP32 SIM tablet monograph was observed (United, 2009). For assay, an adequate SIM mass, equivalent to one AW, was accurately weighed (triplicate) and successively diluted with methanol (filtered, if necessary) in order to obtain SIM 40 μg/mL for injection into the chromatograph. The criterion was 90.0-110.0% LA. The dissolution test (first stage only) was performed for six capsule units from each batch (DT80, Erweka, Heusenstamm, Germany) with USP apparatus 2 (paddle) at 75 rpm for 45 min using stainless steel sinkers (Flowscience, Cotia, SP, Brazil) to keep the capsules at the vessel bottom. Monobasic sodium phosphate at 0.01M containing 0.50% SDS, pH adjusted to 7 (40% w/v sodium hydroxide), 900 mL, 37±0.5 °C was used as the dissolution medium and selected Q value was 75%. Aliquots of 5.0 mL were withdrawn from the dissolution vessels, filtered and injected into the chromatograph. The requirement for the first stage of the dissolution test was that each unit had to release at least 80% LA (Q+5%). A validated RP-HPLC method developed in-house was used to determine SIM in assay, content uniformity and dissolution test on a HP1200 quaternary pump liquid chromatograph (Agilent, Palo Alto, CA, USA) using methanol and 0.1% phosphoric acid (80:20 v/v) as mobile phase, at 30°C, 1.5 mL/min, UV/DAD detection λ 238 nm, with automatic injector fitted at 10 μl and a C8 endcapped column (250x4 mm, 5 μm, Merck, Darmstadt, Germany). All standard and sample solutions were filtered through a 0.45 µm filter membrane (Minisart RC15 Sartorius, Goettingen, Germany) before injection.
Calibration curves were constructed from SIM methanolic solutions (n=3) prepared at 4, 20, 40, 60, 80 μg/mL for assay/content uniformity and from SIM in dissolution medium solutions (n=3) prepared at 2, 10, 18, 26, 34 μg/mL for the dissolution test. The respective curve equations were used to determine SIM in assay/content uniformity and the dissolution test. The R statistical software was used to evaluate the curve equation model, normality and homoscedasticity (α=0.05) by the weighted least squares method, Shapiro-Wilk and Levene tests, respectively (Souza, Junqueira, 2005). Data were treated by studentized residual model in order to remove outliers (residues greater than 3.0) where necessary. Intercept, correlation coefficients (r) and % RSD were calculated and the chromatographic parameters of asymmetry (As), retention factor (k) and retention time (t) were observed (Green, 1996; Jenke, 1996; Snyder, Kirkland, Glajch, 1997; United, 2009a). Results were considered significant when the corresponding p value was less than 0.05.
Selectivity was evaluated through peak purity analysis by UV/DAD spectra of capsule samples. In a repre-sentative capsule sample (acquired from the university pharmacy, rather than the 30 pharmacies), SIM 10, 20 and 40 mg correspondent masses were adequately diluted to obtain precision evaluation at three levels of concentrations: 20, 40, 80 μg/mL (n=3), respectively. Accuracy was assessed by recovery of SIM standard (10, 20, 40 mg, n=3) added to SIM capsule sample solution and properly diluted within the linear range (20, 40, 80 μg/mL). Robustness was assessed by variations in flow rate (±0.1 mL/min), methanol ratio (±2%) and temperature (±5 °C) using SIM 40 μg/mL (n=5).
RESULTS AND DISCUSSION
The qualitative composition of all donated SIM capsule batches were provided by the respective pharmacies. Compounded capsule unit price (Table I) ranged from US$0.13 to US$0.27 among the pharmacies, a cost approximately 5.6% to 11.7%, respectively, of Zocor® tablet unit prices (US$2.30). None of the capsule batches showed any problems regarding physical aspect.
Satisfactory results were obtained for precision and accuracy (Table II) with RSD values less than 2.0% and recovery levels between 98.0-102.0%, respectively. The HPLC method was shown to be robust, since there was no statistical difference by ANOVA (p value>0.05) after variation in flow rate (p=0.71), methanol ratio (p=0.06) and temperature (p=0.11).
The response-concentration relationship for assay/content uniformity and dissolution test curves obtained by the weighted least squares method was expressed by a quadratic and linear equation, respectively. Both curves demonstrated adequate normality (Shapiro-Wilk) and homoscedasticity (Levene) for p value>0.05. Intercept was not significantly different from zero (p value>0.05) for the quadratic model for assay/content uniformity. In cases of significant p value less than 0.05, the percentage of the intercept (relative to the 100% analyte level) up to ±2% is accepted, as observed in the linear model for the dissolution test (Green, 1996; Jenke, 1996). Correlation coefficients (r) were greater than 0.999 for SIM assay/content uniformity curve (Jenke, 1996) or greater than 0.98 for the SIM dissolution curve (United, 2009a) and in both cases, RSD values were less than 2.0% (Jenke, 1996). Results of regression analysis are summarized in Table III.
SIM peak eluted with retention factors, k 2.896 (5.622 min) and 4.613 (5.676 min) (k>2), asymmetry factors 0.96 and 1.02 (As<1.2) for assay/content uniformity (Figure 2a) and dissolution test, respectively (Figure 2b) were appropriate (Snyder, Kirkland, Glajch,1997).
The weight determination test results for the thirty batches are shown in Table IV. Four batches (P12, P17, P19 and P20) had to be retested by the removal of content, whereas one batch (P19) did not meet the weight requirements because it contained more than two units (five) with an individual variation greater than 10%AW. Hence, P19 batch showed problems with homogeneity of powder distribution inside the capsules. For the disintegration test, only batch (P4) did not meet the criteria because its capsules did not disintegrate at all within 45 min. The capsules ended swollen and soft suggesting a formulation problem, probably related to a high percentage (30% w/w) of carboxymethylcellulose (CMC), a gel forming agent (Rowe, Sheskey, Quinn, 2009).
For content uniformity (n=30, Table IV), only nineteen (63.3%) batches met the requirements of within 85.0-115.0% LA (87.2-106.3%) and RSD values were less than or equal to 6.0 (1.9-6.0%). Ten batches (P4, P10, P12, P18, P19, P21, P22, P27-29) out of eleven, which failed the test, had an RSD greater than 6.0% (6.2-19.7%) and one batch (P25) had three units below 85.0% LA despite having a RSD lower than 5.0%. These problems related to high %LA variability reflected either inadequate powder homogenization or poor capsule powder distribution leading to drug content differences between units within the same batch. Assay results (Table IV) show that twenty-one batches (70%) met the criteria 90.0-110.0% LA (90.74 to 105.37%) and RSD was less than 2.0% (0.2 to 1.8%). All nine batches (P1, P3, P9, P11, P12, P18, P24, P25, P28) that failed the test showed %LA less than 90.0 but greater than or equal to 85.5%. In some cases, the problem was due to the fact that a purity correction factor may not have been established for the raw material used.
Dissolution test results (Table IV) were evaluated according to SIM % average release and RSD values: 27 batches met the acceptance criteria with individual values greater than or equal to 80% LA (20 mg SIM). All three batches (P4, P12, P18) that failed the test showed high RSD values (14.9, 16.9, 24.6%). Batch P4, whose capsules contained a high CMC percentage (30% w/w) showed very low drug release (<12.7%) for all units. This suggests a serious formulation problem, leading to a large quality discrepancy and hence, drug inefficacy. In summary, out of 30, only 14 (46.6%) batches met the requirements for all quality control tests, encoded P2, P5-8, P13-17, P20, P23, P26, P30. The most common problem was related with content uniformity, occurring in 68.7% of non-approved batches. This finding represents a major concern for the regulatory authorities since it is related with low quality of powder homogenization and its distribution in the capsules, in an essential practice in compounding pharmacies. The second most frequent problem was observed for SIM assay, which occurred in 56.2% of non-approved batches. This may possibly be explained by the lack or inappropriate use of a correction factor due to a raw material with lower purity. Low %SIM release after dissolution test occurred in 18.7% of non-approved batches. These results are closely related to the content uniformity results, since all such batches also showed high RSD values greater than 10.3% for content uniformity test. Weight determination and disintegration problems occurred in isolated batches. Therefore, the conditions and acceptance criteria established for pharmaceutical control tests applicable to SIM compounded capsules are important to evaluate the quality of distinct batches traded not only locally, but also, nationwide. These tests and their specifications have been suggested to devise a SIM capsule monograph, as guidance for pharmaceutical quality control of these products to be included in the latest edition of the Brazilian Pharmacopeia. Although drug compounding activities in Brazil have been regulated by ANVISA for the last ten years, by means of several acts and their updates, content uniformity problems can be easily avoided by rigorous quality requirements and personnel training. In addition, considering that each batch had been acquired by one patient, 53.3% of these individuals would have had their treatment compromised due to lack of quality compliance.
The authors acknowledge Fapemig and CAPES for funding support, and the Pharmacy undergraduate Amanda Leão dos Santos for laboratory assistance.
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Received for publication on 17th December 2010
Accepted for publication on 30th May 2011
* Correspondence: F.D. Marques-Marinho. Departamento de Produtos Farmacêuticos, Faculdade de Farmácia, Universidade Federal de Minas Gerais. Av. Pres. Antônio Carlos, 6627 - 31270-901 - Belo Horizonte, MG, Brasil. E-mail: firstname.lastname@example.org