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Research Article - (2013) Volume 4, Issue 6

An Explicit Review on Quantitative Estimation of Candesartan Cilexetil Employing Various Analytical Techniques

Shantanu Bandyopadhyay1*, Lohit Bhuria1 and Devi Lal2
1University Institute of Pharmaceutical Sciences,UGC Centre of Advanced Studies, Panjab University, Chandigarh 160 014, India
2Technical Assistant, DST-FIST Lab, University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh 160 014, India
*Corresponding Author: Shantanu Bandyopadhyay, University Institute of Pharmaceutical Sciences UGC Centre of Advanced Studies, Punjab University, Panjab University, Chandigarh 160 014, India Email:

Abstract

Angiotensin II Receptor type 1 antagonists have been widely used in treatment of various disorders like hypertension, heart failure, myocardial infarction and diabetic nephropathy. Over the years, varied analytical methods were developed both in biological fluids as well as dosage forms in order to estimate their desired pharmacological activity. Candesartan being highly lipohpilic with variable oral bioavailability, its estimation in biological fluids is very critical for establishing its subsequent therapeutic efficacy. A few UV spectrophotometeric and volatmmetric techniques have been reported to estimate candesartan in bulk formulations. Additionally, capillary electrophoresis methods provided qualitative and quantitative estimation of candesartan with a few methods being systematically optimized using experimental designs. Ultimately, an overview of different HPLC and LC-MS/MS methods explained the importance of the methods while estimating candesartan in various biological fluids (e.g. plasma, urine, etc.) as well as other studies like, stability studies. This review provides a bird’s eye-view on the various analytical techniques employed for determination of candesartan in both in vitro and in vivo conditions.

Keywords: Candesartan; Spectrophotometry; HPLC; LC-MS/MS; Biological fluids

Introduction

Candesartan cilexetil (CC) is a long acting nonpeptide prodrug which selectively inhibits Angiotensin II Receptor type 1 causing reduction in blood pressure without altering the heart rate. Hence, it is therapeutically indicated in the chronic treatment of hypertension [1,2]. Further, it is effective and well tolerated when used either as monotherapy or in combination with other antihypertensive agents in patients with mild, moderate or severe hypertension [3,4]. It was approved by USFDA in September 2000 and presently marketed by AstraZeneca and Takeda Pharmaceuticals. Recent reports indicated its increased use with the published data signifying its benefit in the treatment of stroke, heart failure, diabetic renal disease and diabetic retinopathy [5]. Being a highly lipophilic drug (Log P = 6.1) with low aqueous solubility of 5×10-5 g.L-1, the drug is classified as BCS class II drug [6-8].

Clinical Background

The absolute oral bioavailability of CC is variable and reported to be about 15% and 42% due to incomplete absorption [8-10]. Also, the relative bioavailability of CC (8 mg tablet) was found to be 34% when compared to oral solution (8 mg). This low bioavailability is due to poor aqueous solubility leading to slow rate of absorption construing that dissolution is the limiting step for the rate and extent of absorption. In a study with single and repeated once-daily doses of CC in the dose range of 2-16 mg carried out in both younger (19-40 years) and elderly (65-78 years) healthy volunteers various pharmacokinetics parameters were determined. It was observed that AUC and Cmax showed doseproportional increment in the dose range of 2-16 mg indicating linear pharmacokinetics. Non-compartmental models do not appear to be appropriate for the analysis of candesartan pharmacokinetics. The terminal elimination half-life of CC was estimated in the range of 4 to 9 h. The time to reach peak candesartan concentrations (Tmax) following tablet intake was approximately 4 h at all dose levels. Also, the plasma protein binding in humans was quite high (>99%) with relatively low volume of distribution in healthy subjects (i.e., 0.13 L.kg-1). After reaching systemic circulation candesartan is cleared mainly by kidneys and to a smaller extent by biliary or intestinal routes. Clinically effective doses of CC ranged between 8 and 32 mg. The antihypertensive effect with CC monotherapy increases with the dose but never exceeds 60% at a daily dose of 16 mg. However, at doses up to 32 mg day, antihypertensive effect did not increase further [9,11-14].

Physicochemical Properties

Prior to the initiation of CC analysis, it is imperative to have a holistic knowledge of its structure as well as other physicochemical characteristics. CC is a tetrazole derivative and chemically is (+)-1-(cyclohexyloxycarbonyloxy) ethyl 2-ethoxy-1-[[2'-(1Htetrazol- 5-yl)biphenyl-4-yl]methyl]-1H-benzimidazole-7-carboxylate (Figure 1) [15,16]. The chemical structure consists of a lipophilic substituent, i.e., tetrazolyl biphenylmethyl moiety and a carboxyl group [17]. Its molecular weight is 610.66 g.mol-1 with empirical formula C33H34N6O6. It is a white to off-white powder which is highly soluble in dimethylsulfoxide; sparingly soluble in methanol, ethanol or physiological saline solution and practically insoluble in water. The partition coefficient (Coctanol/Caqueous) at pH 1.1, 6.9 and 8.9 is >1000 indicating high lipophilicity character [18]. The prodrug is a racemic mixture containing one chiral center at the cyclohexyloxycarbonyloxy ethyl ester group. Following oral administration, CC undergoes hydrolysis at the ester link to form the active drug, candesartan, which is achiral [19,20]. Candesartan in turns is converted to one inactive metabolite [13].

pharmaceutica-analytica-acta-candesartan-cilexetil

Figure 1: Chemical structure of candesartan cilexetil.

Quantification Methods

The pKa value of a drug is important as it is associated with the various biological processes such as body absorption, tissue distribution and elimination. Besides, the information about dissociation constants is also necessary to choose the optimal conditions for the extraction of these drugs from body fluids, which is an essential step to develop analytical methods for their determination [21]. As such a good correlation could be established by knowing the structure and the different acid-base species which in turn affects the absorption rate, the distribution profile and the excretion percentage. CC contains two acidic functional groups: a carboxyl and tetrazole moieties with their respective pKa values were calculated to be 6.0 [22]. In another citation the pKa values for carboxyl and tetrazole moieties were reported to be 5.3 [12].

Till date, many analytical methods have been developed for the quantification and determination of candesartan in biological fluids and pharmaceutical dosage form. In most of the cases, the analysis in biological fluids were carried our employing HPLC or LC-MS/MS techniques. However, there are a few reports wherein CC has been determined using UV spectrophotometry and voltametric methods.

In one of the UV spectrophotometric methods, CC was assayed by first derivative and ratio derivative spectrophotometry in a mixture containing hydrochlorothiazide. Calibration curves were established in the range of 6.0-38.0 μg.mL-1 for CC and the method was found to be linear, precise and selective. The method was subsequently successfully applied to the pharmaceutical dosage form containing the abovementioned drug combination which also showed non-interference by the excipients [23]. Another UV spectrophotometric method was developed for CC estimation in bulk and formulations. Linearity of the method was validated in the range of 10.0-90.0 μg.mL-1. The stability of CC was analyzed under various forced degradation conditions like, acid, alkali and neutral hydrolysis, oxidation, dry heat, UV light and photolytic degradation Subsequently, the method was found to be simple, sensitive and reliable with good precision and accuracy [24]. Another method focused on first derivative UV quantitative analysis in tablet dosage forms during in vitro dissolution testing. The highlight of the method was that the LOQ was 3.06 μg.ml-1 when analyzed in the concentration range of 6.00-32.00 μg ml-1. Also, the percent recovery was also high concluding that the method passed all the parameters of quality control, i.e., accuracy, precision, sensitivity and selectivity [25].

Voltammetry is basically an electroanalytical method which is used to analyze an analyte by measuring the current with varying potential [26]. The reported methods utilized phosphate buffer as the supporting electrolyte. In the first reported method, CC was analyzed with different types of voltammetric techniques viz. cyclic, linear sweep, differential pulse, adsorptive stripping differential pulse, square wave and adsorptive stripping square wave. The analysis was carried out in the pH range 1.5-11.00. Further, differential pulse and square wave voltammetry techniques were studied to obtain a good sensitivity of the method. Finally, the method was validated and successfully applied for the analysis of CC tablets [27]. A simple and sensitive rapid adsorptive stripping voltammetric method was also developed for estimation of CC in pharmaceutical formulations. The linearity was observed between 0.25 and 1.34 μg mL-1. The method was finally validated for linearity, precision, accuracy and recovery [28]. However in another method, the authors used only squarewave adsorptive stripping square method for determination of CC in bulk and pharmaceutical formulations. The method involved a modification wherein CC was complexed with copper, Cu (II). Various experimental and instrumental parameters were investigated and optimized. Subsequently, the method was validated in terms of linearity, sensitivity, precision, accuracy, recovery, selectivity, robustness, and ruggedness [29]. Recently, a newly modified method based on continuous coulometric fast fourier transformation cyclic voltammetry was developed for CC determination. In this technique, a new sensor was designed based on silicon carbide nanoparticles and graphene nanosheets hybrid mixed with ionic liquid (1-Butyl- 3-methylimidazolium hexa fluorophosphate ([bmim][PF6]) on a glassy carbon electrode. The sensor exhibited good accuracy with high sensitivity and repeatability. Even, it had 55 days of long term stability with a decrease of 2.3% in the response. Scanning electron microscopy and impedance spectroscopy was used to characterize the electrode surface [30].

Capillary electrophoresis, also known as capillary zone electrophoresis separates the ionic species based on their charge, frictional forces and hydrodynamic radius [31]. Similar to voltammetry technique, phosphate buffer have been used as running electrolyte in all the reported capillary electrophoresis methods. Also, the detection of the ionic samples has been set at 214 nm using UV detector. Except one method, in all the other methods, a constant volateg of 25 kV have been applied. To identity the sample components the instrument can be coupled with mass spectrometers or surface-enhanced raman spectroscopy. Finally, the reported methods have been validated for linearity of response, precision, reproducibility, and accuracy. Table 1 illustrates the four methods employed along with the various experimental conditions. Additionally, the technique is optimized using experimental design methodologies by applying three-level and four-factor full-factorial design in two cases and three-level and threefactor face-centred central composite design in one analysis [32-34]. Also, CC was determined, both qualitatively and quantitatively, using micellar electrokinetic capillary chromatographic [34,35].

S. No. Running Electrolyte Solvent Capillary Voltage Instrument Detector Reference
1. 50 mM potassium dihydrogen phosphate:boric acid (25:75 v/v, pH 5.5) and at a 5 methanol Methanol Fused silica +25 kV Waters Quanta 4000 UV (214 nm) [32]
2. 60 mM sodium phosphate buffer (pH 2.5) 1 M HCl Fused silica 25 kV Crystal CE UV (214 nm) [33]
3. 10–40 mM of mixture of a disodium hydrogenphosphate solution and a sodium dihydrogenphosphate solution (pH range 6.0–7.5) 0.1 MNaOH Fused silica 10 kV Waters Quanta 4000 UV (214 nm) [34]
4. CZE Method: 60 mM sodium phosphate buffer (pH 2.5) 1 M HCl Fused silica 25 kV Crystal CE UV (214 nm) [35]
MEKC Method: 55 mM sodium phosphate buffer (pH 6.5) 0.1 MNaOH

Table 1: An updated account on various Capillary Electrophoresis methods employed for the estimation of Candesartan cilexetil.

Although, the main advantages of previous mentioned methods are shorter analysis time, lesser solvents, low cost of analysis and widespread availability of the apparatus yet they cannot be applied for analysis in biological samples. Hence, in order to estimate CC in biological systems, it was imperative to develop HPLC and LC-MS/MS methods.

In the following discussions, different HPLC based analytical techniques were elaborated for the determination of CC in the biological fluids and dosage forms. Table 2 enumerates the various HPLC methods employed for CC estimation, till date.

S. No. Type of Media Column Mobile Phase Detector Chromatographic conditions Reference
1. Human serum YMC ODS (23 × 4.0 mm) YMC ODS (150 × 4.6 mm) Phase A: Acetonitrile and potassium dihydrogen phosphate (20 mM) in ratio of 60:40, pH 4.0
Phase B: Acetonitrile and dihydrogen phosphate (20 mM) in ratio of 60:40, pH 6.0  		 UV (229 nm) Flow rate: 1.0 mL.min-1 Temperature: 40°C [36]
2. Human serum and urine Inertsil ODS-2 ( 150 × 4.6 mm, 5μm) First column: 0.02 M potassium  dihydrogen phosphate Acetonitrile (40:60) adjusted to pH 4.0 with 85 orthophosphoric acid
Second column: 0.02 M potassium  dihydrogen phosphate Acetonitrile (40:60) adjusted to pH 6.0 with 1M NaOH		 Fluorescence detector (Excitation and Emission wavelengths set at 270 and 390 nm) Flow rate: 1.0 mL.min-1 Temperature: 40°C [37]
3. Human plasma and urine Spherisorb S3P (100 × 4.6 mm, 3 μm Hichrom) Candesartan (Plasma):
100 ml citrate buffer (pH 3.1, I=0.5 containing 50 mM TBA), 185 ml acetonitrile, 180 ml methanol and diluting to 1000 ml with water		 Fluorescence detector (Excitation and Emission wavelengths set at 265 and 395 nm) Flow rate: 0.9 mL.min-1 Temperature: room [40]
Candesartan cilexetil (Plasma & urine):
200 ml phosphate buffer (pH 2.8, I=0.1 containing 12.5 mM TBA), 420 ml acetonitrile and diluting to 1000 ml with water		 Flow rate: 1.0 mL.min-1 Temperature: room
Candesartan (Urine):
Phase A: 200 ml phosphate buffer (pH 2.8, I=0.1 containing 12.5 mM TBA), 200 ml acetonitrile and diluting to 1000 ml with water
Phase B: 200 ml phosphate buffer (pH 2.8, I=0.1 containing 12.5 mM TBA), 600 ml acetonitrile and diluting to 1000 ml with water		 Flow rate: 1.0 mL.min-1 Temperature: room
4. Human plasma Novapak guard column (20 × 39 mm, 4 μm) muBondapak (300 × 3.9 mm, 10 μm) Acetonitrile (5 mM) acetate buffer (pH 4) Fluorescence detector (Excitation and Emission wavelengths set at 250 and 375 nm) Flow rate: 1.0 to 1.2 mL.min-1 Temperature: room [41]
5. Human plasma and urine Betasil (250mm × 4.6mm, 5μm) Acetonitrile and  Sodium acetate buffer solution (5mM, pH 3.5) in the ratio of 40:60) PDA (250 nm) and fluorescence  (Excitation and Emission wavelengths set at 250 and 380 nm) Flow rate: 1.0 mL.min-1 [42]
6. In vitro dissolution Inertsil ODS-3 (250 × 4.6-mm, 5 μm) 0.02 M monobasic potassium phosphate, acetonitrile, and triethylamine in the ratio of 40:60:0.2 (pH adjusted to 6.0 using phosphoric acid) UV (254 nm) Flow rate: 2.0 mL.min-1 Temperature: 25°C [43]
7. Stability studies Hypersil ODS (250 × 4.6 mm, 5 μm) 0.02M Potassium dihydrogen phosphate solution and acetonitrile (2:8), pH 4.0 was adjusted with 85 phosphoric acid UV (254 nm) Flow rate: 1.0 mL.min-1 Temperature: ambient [44]
8. Drug analysis Zorbax SB-Phenyl 0.1 mol.L-1 sodium acetate (pH 5.5), acetonitrile and methanol in 10:9:6 v/v/v ratio UV (230 nm)   [45]
9. Drug analysis Hypersil ODS (250 × 4.6 mm, 5 μm) Tetra butyl ammonium hydrogen sulphate 10 mM (pH 3.37): methanol (15:85) UV (270 nm) Flow rate: 1.0 mL.min-1 Temperature: ambient [46]
10. Drug analysis Hypersil Phenyl 2 (250 × 4.6 mm, 5 μm) 0.02 M potassium dihydrogen phosphate, methanol, and triethylamine (25:75:0.2 v/v), pH 6.0 ± 0.1 was adjusted by addition of 10 orthophosphoric acid UV (271 nm) Flow rate: 1.0 mL.min-1 Temperature: room [47]
11. Everted gut sac (Rat) Shim-pack VP-ODS (150 × 4.6 mm, 5 μm) Acetonitrile: Methanol: water: glacial acetic acid (40:35:25:0.1 v/v), pH 6.8 UV (255 nm) Flow rate: 1.0 mL.min-1 Temperature: ambient [48]

Table 2: An updated account on various HPLC analysis employed for the estimation of Candesartan cilexetil.

CC was estimated employing column-switching HPLC wherein the zone of analyte’s retention obtained from earlier column is transferred to another column by increasing the pH of the mobile phase. The method was used for determination CC and its metabolites in human serum and urine with good linearity, precision, accuracy and low LOQ. The versatility of method was further established from the results of stability studies [36]. In another column-switching method, using an FCV-2AH six-port valve, CC along with its two metabolites was analyzed in human serum. The metabolites were also analyzed in urine by gradient elution mode HPLC. The method were later on applied for conducting the clinical trials of CC [37].

A placebo-controlled, double-blind, four way crossover design for oral doses of 4, 8 and 16 mg of CC was carried out in healthy human volunteers. Following this blood samples were withdrawn periodically and various pharmacokinetic parameters were calculated. The study indicated that CC shows dose-dependent behavior in pharmacokinetic responses [38]. In another double-blind, crossover study, 12 healthy male volunteers received daily oral doses of 8 mg CC. A liquid chromatography assay was employed to determine the plasma concentrations of CC and subsequent pharmacokinetic parameters [39].

Owing to extensive pharmacokinetic and clinical studies, a fast and easy HPLC method was reported for determination of CC in biological fluids. In one of the assays liquid-liquid extraction was carried out with dichloromethane-diethyl ether (1:4, v/v) and analyzed with fluorometric detection. The method was applied to human plasma and urine samples which were further used for biopharmaceutical and clinical studies in man. For efficient extraction of samples, a guard column was also utilized. The method was quantified with high precision and strikingly, LOQ was found to be quite low. Also, the CC samples were stable under different storage conditions [40].

CC was also analyzed under acidic conditions wherein the analyte was extracted from plasma by means of solid-phase extraction using C8 cartridges. This assay was successfully applied to plasma samples obtained from hypertensive patients [41]. In a modified solid-phase extraction, a poly (methacrylic acid-ethylene glycol dimethacrylate, MAA-EGDMA) monolithic capillary was used for extraction of CC from human plasma and urine. The method was demonstrated to be robust and biocompatible by using direct injections of biological samples [42].

In order to enhance the oral bioavailability of CC, a solid selfmicroemulsifying formulation was prepared. Initially, a liquid system was formulated using various combinations of lipid, emulgents and cosolvents. The liquid emulsifying system was then converted into free flowing powder by adsorption on solid carriers, i.e., microcrystalline cellulose and colloidal silicon dioxide. Finally in order to estimate the amount drug released during in vitro dissolution studies, a HPLC method was employed [43].

A HPLC method was employed for assessing the stability of CC in various types of cyclodextrin based formulations. It was found that CC was stable at ambient conditions for 3 years as well as when stored in open containers at 40°C/75% RH and 50°C/75% RH for 3 months and 1 month, respectively. Also, Exposure to sunlight and UV light for 1 month similarly showed no loss in potency and absence of any degradation product [44].

In order to analyze the CC content in bulk substances and tablets, a gradient based HPLC method in isocratic mode was developed. During this process, 100.40% of CC was recovered from simulated tablets [45]. There are reports of two other simple and sensitive HPLC methods being developed and validated for determining CC in pharmaceutical dosage forms. Like the previous one, these methods were also run on isocratic mode [46,47]. A HPLC method was also applied for estimating the CC content during everted gut sac technique [48].

Over the years, many methods have been developed for the determination of CC in biological samples and pharmaceutical dosage forms based on LC-MS/MS method. It is a technique that combines the physical separation capabilities of liquid chromatography (or HPLC) with the mass analysis capabilities of mass spectrometry. Generally its application is focused on the general detection and potential identification of molecules or derivatives in a complex mixture [49-51]. Table 3 provides an account of various methods for the estimation of CC using LC-MS/MS method.

S. No. Type of Media HPLC Column HPLC Mobile Phase Mass Analyzer Chromatographic conditions Reference
1. Rat plasma and bile AM-312 (ODS, 150 × 6 mm, 5μm) Water-acetonitrile-trifluoroacetic acid (70 : 30: 0.1v/v) Finnigan MAT (QqQ) Flow rate: 1.0 mL.min-1 Temperature: ambient [52]
2. Rat plasma ACE C18 column (50 × 4.6 mm, 5 μm) 10 mM ammonium acetate:acetonitrile (20:80, v/v) MDS Sciex API 4000 (Q) Flow rate: 0.5 mL.min-1 Temperature: 40 ± 2°C Detection: PDA (254 nm) [54]
3. Human plasma Synergy Polar RP (150 × 2 mm, 4μm) Solvent A: 0.1 formic acid (v/v) with 1 mmol/L ammonium formate Solvent B: acetonitrile: 0.1 formic acid 95:5 (v/v) with 1 mmol/L ammonium formate API 365 (QqQ) Flow rate: 0.25 mL.min-1 Temperature: 40°C [55]
4. Rabbit eyes Capcell Pak (4.6 × 250 mm, 5 μm) Acetonitrile and water (0.1 formic acid) 6410 (QqQ) Flow rate: 1.0 mL.min-1 Temperature: room [57]
5. Stability studies Luna C18 (150 × 4.6 mm, 5 μm) Acetonitrile and potassium dihydrogen orthophosphate buffer (pH 2.8; 0.01M) in a gradient mode MicrOTOF-Q (TOF) Flow rate: 1.0 mL.min-1 Temperature: room Detection: PDA (254 nm) [58]
6. Impurity profile Kromasil cyano column (250 × 4.6 mm, 5 μm) Water adjusted to pH 3.0 with TFA (A) and acetonitrile (B) in a gradient mode PolarisQ (IT) Flow rate: 1.0 mL.min-1 Temperature: room Detection: PDA (210 nm) [59]
7. Human plasma BEH C18, 1.7 μm column (analysis performed with Acquity UPLC) 0.1(v/v) formic acid in Distilled water and 0.1(v/v) formic acid in acetonitrile (60: 40, v/v) Micromass Quattro Premier XE Flow rate: 0.4 mL.min-1 Temperature: room [60]
8. Rat plasma Zorbax SB-C18 (150 × 4.6 mm) with a C18 guard column (4 × 3.0 mm, Phenomenex) Methanol and 5 mM ammonium acetate (50:50 v/v) MDS Sciex API 4000 Flow rate: 0.6 mL.min-1 Temperature: room Detection: PDA (254 nm) [61]

Q: Single quadrupole, QqQ: Triple quadrupole, IT: Ion trap, TOF: Time of flight, Q-TOF: quadrupole-time of flight

Table 3: An updated account on various LC-MS/MS analysis employed for the estimation of Candesartan cilexetil.

A combined electrospray and tandem mass spectrometry were used to characterize the conjugated metabolites (glucuronides) of CC in the plasma and bile of rats. This analysis was conducted to indentify the positional isomers with respect to the binding site of glucuronic acid. Thus, the simple chemical derivatization indicated the detailed structure of conjugated metabolite [52]. This combined spectrometry was also used to develop a method in human plasma with respect to simple sample clean-up and investigation of ion suppression effects. The developed method showed good precision and accuracy at different concentrations. The calculated LOD was quite low and CC was stable during the analytical process [53].

A high-throughput bioanalytical method for the analysis of CC in human plasma was developed and validated according to US FDA guidelines. The method was subsequently validated for precision and was stable under standard conditions with its ability to be applied successfully to oral pharmacokinetic study in humans [54].

During the development of a solid phase extraction procedure for the chromatographic determination, lack of linearity and reproducibility was observed for CC. As such a stability study was performed and it was found that lack of linearity and reproducibility was based on hydrolysis and trans-esterification processes. Subsequently, a detailed study was performed to assure that labile drugs containing ester groups remain unaffected [55].

In a study to evaluate the impact of high pH modifiers on the sensitivity of CC, LC-MS/MS under positive ESI (ESI+) was employed. The signal enhancement was two-fold compared with acidic modifiers and thus facilitated the development of a bioassay for the quantification of CC [56].

A method based on LC-MS/MS was developed to investigate the intravitreal toxicity and pharmacokinetics of candesartan and subsequent calculation of CC concentration in rabbit eyes [57].

A detailed stress degradation studies was conducted as per the ICH conditions of hydrolysis (acidic, basic and neutral), photolysis, oxidation and thermal stress. During the study, maximum degradation was observed on hydrolysis, especially in the neutral condition, followed by significant photolytic degradation. However, it was stable to oxidative and thermal stress. The method was able to provide an updated and comprehensive fragmentation behavior and degradation profile of CC [58].

During the impurity profiling in bulk drug samples, four impurities were detected in CC by HPLC and LC/MS. An optimized method using liquid chromatography coupled with electrospray ionization ion trap mass spectrometry was developed to elucidate the structures of these unknown impurities. The plausible mechanism for the formation of impurities was also discussed [59].

In an open-labeled, randomized, single dose, crossover design involving 40 healthy volunteers, various parameters of pharmacokinetics were determined. Also, the bioequivalence of two CC 16 mg formulations were evaluated. The single dose study concluded that the test and reference products met the regulatory criteria for bioequivalence in the health volunteers [60].

Owing to poor aqueous solubility, CC undergoes incomplete intestinal absorption leading to low oral bioavailability. A novel CC loaded nanoemulsion was designed to improve the intestinal absorption. The concentration of active candesartan in rat plasma was determined by LC-MS/MS method. The experimental results showed an overall 10-fold improvement in oral absorption of insoluble CC and thus proving its potential for clinical applications [61].

Conclusion

Overall, various techniques were employed for the estimation of CC. Although the techniques viz. UV spectrophotometry, voltammetry and capillary electrophoresis are simpler and easier to apply yet they could not be applied for estimation in biological matrixes. HPLC method is an usual tool for the researcher, being mostly employed for routine analysis purpose. LC-MS/MS is used due to its high sensitivity and exceptional specificity compared to other method esp. when the sample is ionized and require shorter analysis time. Also, the optimum concentrations for therapeutic efficacy of many drug(s) range from a few nanograms to hundreds of nanograms per milliliter. In such cases, LC-MS/MS method provides a quality standard as per USFDA for therapeutic drug monitoring, clinical and forensic toxicology of drugs. Conclusively, modern instruments like, HPLC and LC-MS provides a simple, rapid and reliable method for quantification of candesartan and/or its metabolites which ultimately facilitate the in vitro and in vivo evaluations of candesartan.

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Citation: Bandyopadhyay S, Bhuria L, Lal D (2013) An Explicit Review on Quantitative Estimation of Candesartan Cilexetil Employing Various Analytical Techniques. Pharm Anal Acta 4:254.

Copyright: © 2013 Bandyopadhyay S, 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.