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Brazilian Journal of Pharmaceutical Sciences

On-line version ISSN 2175-9790

Braz. J. Pharm. Sci. vol.51 no.4 São Paulo Oct./Dec. 2015 


A green approach for the quantification of daptomycin in pharmaceutical formulation by UV spectrophotometry

Eliane Gandolpho Tótoli1  * 

Hérida Regina Nunes Salgado1 

1School of Pharmaceutical Sciences, Universidade Estadual Paulista Júlio de Mesquita Filho", UNESP, Araraquara, SP, Brazil


Daptomycin is the first approved drug from a new class of antimicrobials, the cyclic lipopeptides, and is a very important antimicrobial agent in current clinical practice. Currently, there are no "green" analytical methods described in the literature to analyze the typical pharmaceutical dosage form of daptomycin. Thus, the aim of this work was to validate an environment-friendly spectrophotometric method in the UV region, for the analysis of daptomycin as a lyophilized powder. Water was used as diluent and the analyses were carried out on a spectrophotometer at 221 nm. The method met all validation requirements of the ICH guidelines, over a concentration range of 6-21 µg mL-1. A Student's t-test demonstrated that the proposed method was comparable to an HPLC method previously validated. Thus, the validated spectrophotometric method could quantify daptomycin in a powder form for injectable solutions, while being an economical, rapid, and "green" alternative for routine analysis in quality control.

Uniterms: Antimicrobials/quality control; Daptomycin/determination; Spectrophotometry/UV region/quantitative analysis; Spectrophotometry/green analytical method


A daptomicina é o primeiro membro aprovado de uma nova classe de antimicrobianos, os lipopeptídeos cíclicos, e é muito importante para a prática clínica atualmente. Não existem métodos analíticos "verdes" descritos na literatura para a análise da daptomicina na forma farmacêutica. Desta forma, o objetivo deste trabalho foi a validação de método espectrofotométrico na região do UV ambientalmente favorável para análise da daptomicina em pó liofilizado. A água foi escolhida como diluente e as análises foram realizadas em 221 nm. O método atendeu a todas as exigências de validação dos guias do ICH, na faixa de 6-21 µg mL-1. Teste t de Student mostrou que o método proposto é intercambiável com método de HPLC previamente validado. Assim, o método espectrofotométrico validado é capaz de quantificar a daptomicina em pó para solução injetável e é uma opção econômica, rápida e "verde" para análises de rotina do controle de qualidade deste fármaco.

Unitermos: Antimicrobianos/controle de qualidade; Daptomicina/determinação; Espectrofotometria/ região do UV/análise quantitativa; Espectrofotometria/método analítico verde.


It is widely known that microbial resistance is a major problem worldwide. Many bacteria have developed resistance to a large number of antimicrobial agents available on the market; these bacteria are considered challenges for medicine. Methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin resistant enterococci (VRE) are two examples of antimicrobial-resistant microorganisms (Silveira et al., 2006; Wright, 2011). Compounding the problem of antimicrobial resistance, there are few new antimicrobial agents emerging in the market (Wright, 2011).

One recent development in antimicrobial treatment is the introduction of daptomycin into the marketplace (Figure 1). This is the first antimicrobial agent from the cyclic lipopeptide class approved for use in clinical practice in the United States in 2003, and currently in more than 40 countries worldwide (Lopes, 2008; Pirri et al., 2009; Sweetman, 2011).

FIGURE 1 Chemical structure of daptomycin. 

Daptomycin has a mechanism of action that is distinct from all other antimicrobial agents available in the market. For this reason, it is able to overcome the mechanisms of resistance that many resistant strains have developed. It has been used successfully in treating some infections caused by resistant gram-positive bacteria, such as MRSA and VRE. Furthermore, resistance to daptomycin is rare worldwide (Silveira et al., 2006; Picazo et al., 2011; Brunton, Chabner, Knollman, 2012; Chitnis et al., 2013; Sader et al., 2014).

The quality of medicines has always been a concern to the World Health Organization (WHO), because without the assurance that these products meet the standards of quality, safety, and efficacy, worldwide health services can be affected. In addition, governments allocate a substantial part of their health budget to purchasing medicines. For these reasons, the WHO advocates for the availability of a reliable system of quality control of medicines in all countries (WHO, 2007). Thus, worldwide interest in research involving medications is increasing, particularly with respect to their quality control. Research that involves the development of new analytical methods is essential to optimize the analysis of medicines in the industry, and guarantees the quality of products already marketed.

In addition to the concern about the quality of analytical data, there is also concern about the environmental impact of industrial activity. Increasingly, companies are seeking environmentally friendly alternatives to their routine processes, adopting a commitment to reducing, preventing, or eliminating harmful waste. There are actions that companies can take to reduce the environmental burden, including the replacement of analytical techniques that employ organic solvents with techniques that do not (Nolasco, Tavares, Bendassoli, 2006).

A few published studies in the literature describe the development of analytical methods to analyze daptomycin. Most of these studies are directed towards biological fluid analysis by high performance liquid chromatography (HPLC), (Tobin et al., 2008; Martens-Lobenhoffer et al., 2008; Baietto et al., 2010; Gika et al., 2010; Olszowy et al., 2010; Polillo et al., 2010; Verdier et al., 2011; Szultka et al., 2013) and ultra-performance liquid chromatography (UHPLC) (Gikas et al., 2010a; Gikas et al., 2010b; Bazoti et al., 2011; Baietto et al., 2014; Naito et al., 2014). In addition, there are no monographs of this drug in any official compendium. One study using HPLC was found in the literature describing an analytical method for the analysis of daptomycin in its pharmaceutical powdered dosage form (Christ et al., 2014).

Most of the reported analytical methods employed techniques that are not considered ecologically friendly in analytical laboratories. Furthermore, the methods that used liquid chromatography require toxic solvents or high volumes of solvents for drug quantification, which is more expensive and unhealthy for the laboratory staff and the community.

Spectrophotometric instrumental methods are considered simple, fast, inexpensive, and reproducible. In addition, they can be developed without the use of organic solvents, which makes this technique more environmental-friendly (Moreno, Salgado, 2009; Bonfílio, Araújo, Salgado, 2011; Cazedey, Salgado, 2012; Fiorentino, Salgado, 2012; Silva, Almeida, Salgado, 2012; Pedroso, Salgado, 2013; Cazedey, Salgado, 2014; Chierentin, Salgado, 2014; Corrêa, Serra, Salgado, 2014). To our knowledge, there are no studies in the literature that used spectrophotometry to analyze daptomycin.

Considering the importance of daptomycin in clinical practice, and the advantages of spectrophotometric methods, the main objective of the present study was the development of a fast and environmentally friendly ultraviolet (UV) spectrophotometric analytical method for the quantitative analysis of this drug in its lyophilized powder form. As a control, we used a high performance liquid chromatography (HPLC) method, previously developed and validated by our study group, as a comparative method in the determination of this drug.



To perform the spectrophotometric analysis, a ShimadzuTM UV-Vis UV-1800 model spectrophotometer (Shimadzu, Japan) was used. This equipment was connected to a computer loaded with the UV-ProbeTM software. Microsoft Excel (2013) was used to construct the calibration curves. In order to evaluate the robustness of this method, we also used a ShimadzuTM UV-Vis UV mini-1240 model spectrophotometer (Kyoto, Japan).

For comparative HPLC analysis, we used a model 1525 Waters HPLC (Waters Chromatography systems, USA), connected to a Waters 2487 UV/Visible detector, and a manual injector Rheodyne Breeze 7725i with a 20 µL loop (Rheodyne Breeze, USA). The chromatographic separation was carried out using isocratic reversed phase conditions on an Agilent ZorbaxTM C18, 5 µm, 4.6 x 150 mm (Agilent, USA).

The following equipment was also used: 20-200 µL micropipettes (DigipetTM, Brazil) and an H51 analytical scale (Mettler ToledoTM, Switzerland).

Chemicals and reagents

Daptomycin (DPT) reference standard (DPT RS) (purity of 98.00%) was purchased from Sequoia Research Products Company (Sequoia, UK). Samples containing 500 mg of daptomycin, as a lyophilized powder for injectable solution, (CubicinTM, Novartis, USA) were purchased on the market. The pharmaceutical form contains sodium hydroxide as an excipient. For this reason, sodium hydroxide (Vetec, Brazil) was also used. The solvent used was purified water (obtained by reverse osmosis - Millipore, USA). In order to evaluate the robustness of the method, purified water obtained through Milli-Q Plus equipment (Millipore, USA) was also used.

Spectrophotometric measurements

UV-Vis spectra of reference and sample solutions were measured using 1-cm quartz cells, and a fast scan speed. Purified water, obtained by reverse osmosis, was used as blank solution for the spectrophotometric measurements. A 221 nm wavelength was used to develop the present method.

Chromatographic conditions

In order to compare the results of the proposed spectrophotometric method with a reference method, the same DPT batch was analyzed using an HPLC technique previously developed and validated by our study group. We performed this experiment in isocratic mode, and the mobile phase consisted of ethanol and water (55:45; v/v) with the pH adjusted to 4.5 using glacial acetic acid. Chromatographic separation was achieved using an Agilent ZorbaxTM C18 analytical column (150 x 4.6 mm; 5 µm) (AgilentTM, USA). The volume of the injection was 20 µL and the flow rate was 0.6 mL min-1. Room temperature was maintained at 25 ºC. The peak areas detected at 221 nm were defined as analytical signs, with detection at 221 nm.

Preparation of solutions

Stock and working standard solutions

For the preparation of the DPT RS stock solution, 5.0 mg of DPT RS was weighed, then transferred and diluted with purified water to a volume of 50 mL in a volumetric flask, yielding a solution with a concentration of 100 µg mL-1.

Working DPT RS solutions were prepared immediately before use, using purified water to dilute the corresponding stock solution to appropriate concentration levels. For the HPLC analysis, the stock and working standard solutions were diluted with mobile phase.

Stock and working sample solutions

DPT sample stock solution at a theoretical concentration of 100 µg mL-1 was prepared. For this purpose, the average weight of three vials of DPT in powder for injectable solution was calculated. The contents of these vials were mixed, and an amount equivalent to 5.0 mg of DPT was accurately weighted, transferred to the 50-mL volumetric flask, and diluted to 50 mL with purified water, yielding a stock solution of 100 µg mL-1. Appropriate dilutions were made using the same diluent, in order to obtain the working sample solutions. For the HPLC analysis, the stock and working sample solutions were diluted with mobile phase.

Preparation of stock sodium hydroxide solution (placebo)

A solution containing 1000 µg mL-1 of sodium hydroxide was prepared. To prepare the solution, 10 mg of NaOH was weighed, transferred to a 10 mL volumetric flask, and diluted to 10 mL with purified water. Appropriate dilutions were made using the same diluent, in order to obtain a placebo solution with the correct NaOH concentration.

Calculation of the DPT content in the sample

The DPT content in the lyophilized powder sample was calculated by using Equation 1 and its percentage content was calculated by using Equation 2.

Equation 1

Equation 2

where: CS = concentration of DPT in the sample (µg mL-1); CS% = percentage concentration of DPT in the sample; CRS = concentration of DPT RS solution (µg mL-1); AS = absorbance of DPT sample solution; ARS = absorbance of DPT RS solution; Ct = theoretical concentration of DPT in the sample (µg mL-1).

Method validation

The method was validated by determining the following parameters: linearity, precision, accuracy, robustness, selectivity, detection, and quantification limits, in accordance with recommendations in the literature (ICH, 2005; ANVISA, 2010; USP, 2014).


In order to analyze the linearity of the method, three analytical curves, performed on three different days, were evaluated. For this purpose, aliquots of 0.3, 0.45, 0.6, 0.75, 0.9, and 1.05 mL of the stock DPT standard solution were transferred to 5 mL volumetric flasks, and diluted to 5 mL with purified water. This resulted in DPT RS working solutions with concentrations of 6.0, 9.0, 12.0, 15.0, 18.0, and 21.0 µg mL-1. Each concentration was prepared in triplicate (n = 3) and spectrophotometric analysis was conducted at a wavelength of 221 nm. The results were evaluated by linear regression analysis, which was calculated by the least square method, and the linearity was verified by analysis of variance (ANOVA).


Accuracy of the method was evaluated in two different ways: by repeatability and intermediate precision. Repeatability (or intraday precision) was assessed by the analysis of DPT RS working solutions (n = 6) at a concentration of 12.0 µg mL-1, which were prepared and analyzed on the same day and under similar experimental conditions. The percent relative standard deviation (RSD%) of the measurements was calculated and evaluated. Intermediate precision (inter-day and between different analysts) was evaluated by determining DPT content in the samples of lyophilized powder on three different days, and by a second analyst, under the same experimental conditions. RSD% values were calculated between the determinations (ICH, 2005).


Accuracy of the method was determined by measuring the reference standard recovery in triplicate at three levels (R1, R2 and R3), from 80 to 120% of the method concentration (12.0 µg mL-1), according to ICH recommendations (ICH, 2005). For this purpose, the stock solutions of DPT RS and DPT as a powder for injectable solution (100 µg mL-1) were prepared as described in previous sections. From the sample stock solution, aliquots of 0.30 mL were transferred to three 5 mL volumetric flasks. Then aliquots of 0.18, 0.30, and 0.42 mL from the DPT RS stock solution were added. The flasks were then filled with purified water, obtaining solutions with concentrations of 9.6, 12.0, and 14.4 µg mL-1, which is equivalent to 80 (R1), 100 (R2), and 120% (R3) of the working concentration. The mean recoveries, expressed in terms of percent recovery from the pharmaceutical dosage form (CubicinTM 500 mg) by the assay, and the respective relative standard deviation (R.S.D.), were calculated using the equation described by the Association of Analytical Chemists (AOAC) (AOAC, 2002).


In order to evaluate the robustness of the method, the following parameters were individually altered: wavelength (measured at 219 and 223 nm), spectrophotometer (tested with a ShimadzuTM UV mini-1240 model), and an alternative source of water (Milli-Q water). Robustness was evaluated by performing DPT content determinations in the sample of lyophilized powder under the different conditions. The DPT content calculated under the modified conditions was compared with the results obtained under the normal working conditions, according to the RSD% between the results.


In order to evaluate the selectivity of the method, a spectrum obtained with DPT RS solution at a concentration of 12 µg mL-1 was compared with the spectrum obtained with a placebo solution. This determined whether there was any interference from placebo in the DPT analysis.

The DPT RS solution was prepared as described in previous sections. The placebo solution, in turn, was prepared using sodium hydroxide, as it is the only other constituent of the DPT sample excipient. A concentration of 1.03 µg mL-1 was used, equivalent to the concentration of NaOH present in 12 µg mL-1 solution of DPT in lyophilized powder. This percentage of NaOH was calculated according to the average weight of three vials of DPT as a powder for injectable solution. To conduct this test, an aliquot of 51.5 µL from the stock placebo solution at 1000 µg mL-1 was transferred to a 50 mL volumetric flask, the volume was adjusted to 50 mL with purified water, and then the solution was adequately homogenized.

DPT RS and placebo solutions were spectrophotometrically analyzed in the UV region (200-400 nm) and their absorption spectra were compared.

Detection and quantification limits

Detection and quantification limits were calculated based on the intercept standard deviations, and the curve inclinations from the linear regression, as described in the literature (ICH, 2005).

Comparison of methods

In order to compare the spectrophotometric and chromatographic methods, DPT sample content determinations were performed using both methods. The results of the determinations obtained by spectrophotometry in the UV region were statistically compared with those obtained with the HPLC method, using a Student's t test at a level of significance of p < 0.05.


General aspects and method development

Fast and practical analytical methods to quantify daptomycin in either the pharmaceutical dosage form or other forms have not been previously published. The existing methods to analyze this important antimicrobial agent require large volumes of organic solvents and sophisticated equipment. In addition, most of these methods analyze daptomycin in biological fluids, rather than the pharmaceutical dose. In this study, water was chosen as the diluent, since it is inexpensive and not hazardous to laboratory staff or the environment; the choice of this diluent makes the present method economical, safe, practical, and environmental-friendly.

In a recent literature search, an excellent paper detailing the advances made in green pharmaceutical research was discovered (Cue, Zhang, 2009). In this paper, the authors expressed hope, and had high expectations, that the concepts presented will lead to new ecological methodologies to quantify drugs. They discuss case studies of the successful modification of processes to achieve reduced resource requirements, waste generation, or energy consumption. The authors also expressed hope that there will be increased emphasis on green chemistry in pharmaceutical research and manufacturing. In response to environmental concerns, pharmaceutical researchers have concentrated their focus and creative energies towards minimizing and optimizing the environmental impact of their craft. Therefore, with many compounds in queue for therapeutic screening, ecologically friendly changes to the standard processes and current analytical methods that allow for increased throughput are welcome.

To develop the current method, DPT RS UV spectra were obtained in multiple solvents to confirm the suitability of water as a diluent. DPT RS was observed to be soluble in all tested solvents (water, methanol, 0.1 mol L-1 NaOH and 0.1 mol L-1 HCl); the spectra are presented in Figure 2.

FIGURE 2 Ultraviolet absorption spectra of DPT RS solution at a concentration of 12 µg mL-1. The DPT RS was dissolved using the following diluents: a) water; b) methanol; c) 0.1 mol L-1 HCl and d) 0.1 mol L-1 NaOH. 

The maximum absorption wavelength was 221 nm when using water as a diluent. The wavelength was slightly lower, at 220.2 nm, when 0.1 mol L-1 HCl was used as the diluent. The other two solvents tested as diluents, methanol and 0.1 mol L-1 NaOH, had maximum absorptions at 223.6 and 223.0 nm, respectively. The spectra obtained with 0.1 mol L-1 NaOH and 0.1 mol L-1 HCl had a lower absorption peak at the maximum absorption wavelength, suggesting DPT degradation.

Since the spectra were similar between water and methanol, water was chosen as the diluent in the validation of this quantitative method, owing to its economic and environmental advantages. The use of water as a diluent is very relevant to the pharmaceutical industries, since analytical methods that do not use organic solvents for analysis are sought after in order to reduce the impacts of their activities on the environment.

Method validation


Three calibration curves, generated on three separate days, were constructed by plotting the average absorbances at 221 nm with respect to the concentrations. The final analytical curve, constructed using the average of the three analytical curves, yielded a correlation coefficient (r) greater than 0.999 (Table I).

TABLE I Linearity parameters for the determination of DPT 

Parameter Result
Linearity range (µg mL-1) 6.0 to 21.0
Slope 0.0299 ± 0.0003ª
Intercept 0.0095 ± 0.0013a
Correlation coefficient 0.9999 ± 0.0003ª

a Values are reported as mean ± standard deviation (S. D.) of three analytical curves generated on three consecutive days (n = 3).

A linear correlation between the DPT RS concentrations and the respective mean absorbances was observed within the studied range. The correlation coefficient value indicates the high degree of linearity using this method.

In addition, the data were validated using analysis of variance (ANOVA), which revealed significant linear regression, since the Fcalculated (18820.25) was higher that the Fcritical (4.75), while no significant linearity deviation was detected, since the Fcalculated (0.33) was lower than the Fcritical (3.26). This analysis was performed at a significance level of 5% (p < 0.05).


The precision of the method was evaluated in two different ways: repeatability (intraday precision) and intermediate precision (interdays and inter-analyst precisions). The intermediate precision results are presented in Table II. The intraday precision (n = 6) gave an RSD value of 1.20%.

TABLE II Intermediate precision of the spectrophotometric method to determine DPT content 

a mean of three determinations (n = 3)

The RSD% values observed were lower than 1.20%, which confirms the appropriate precision of the method.


The accuracy of the method was determined using a recovery assay performed at three different concentration levels (Table III). The data demonstrates adequate accuracy of the method, since the experimental concentrations were very close to the real values (close to 100%).

TABLE III Accuracy of the spectrophotometric method for the determination of DPT concentration 

Added DPT RS / µg mL-1 DPT RS founda / µg mL-1 Recovery (%) RSD (%) (n = 3) Average recovery (%)
R1 3.60 3.60 100.01 1.43
R2 6.00 5.97 99.58 0.03 99.94
R3 8.40 8.42 100.23 1.06

a average of three determinations.


Robustness of the method was determined, demonstrating the reliability of the analysis regarding small variations in the working parameters. The results show that the validity of the method was maintained, even with small variations in the method´s working conditions (Table IV) (ICH, 2005).

TABLE IV Robustness of the spectrophotometric method for determining DPT concentration 

Variable Range investigated Content (g/vial) Content (%) RSD (%)
Wavelenght (nm) 219 221a 223 0.514 0.519 0.513 102.89 103.74 102.63 0.56
Spectrophotometer UV-Vis ShimadzuTM, UV-1800 modela UV-Vis ShimadzuTM, UV mini-1240 model 0.519 0.513 103.74 102.57 0.81
Source of water Reverse osmosisa Milli-Q 0.519 0.519 103.74 103.76 0.01

a Standard working conditions.

The calculated RSD% values were below 0.81%, proving that small variations in the working conditions will not interfere with the analysis of DPT.


Figure 3 (a) shows the overlap of the spectra obtained with DPT RS solution and placebo solution (NaOH). Figure 3 (b) shows the overlap of the spectra obtained with DPT RS and lyophilized powder solutions. It was observed that the formulation excipient of the DPT in lyophilized powder did not interfere with the UV spectrophotometric method, since the excipient did not have any absorption bands that may have interfered with the analysis of DPT, in the wavelength used in this method. Thus, the selectivity of the method was confirmed.

FIGURE 3 a) Overlap of the absorption spectra of DPT RS (12 µg mL-1) and placebo (NaOH) solutions, using water as the solvent; b) Overlap of the absorption spectra of DPT RS (12 µg mL-1) and lyophilized powder (12 µg mL-1) solutions, using water as the solvent. 

Detection and quantification limits

The limits of detection (LOD) and quantification (LOQ) were calculated to determine the sensitivity of the method. The calculated value for the LOD was 0.14 µg mL-1 and the LOQ was 0.42 µg mL-1. These values indicate the ability of this method to reliably detect and quantify DPT in its pharmaceutical dosage form.

Assay of the pharmaceutical product and comparison between methods

The comparison between analytical methods is an important tool to determine if the procedures are equivalent. Thus, in order to compare the spectrophotometric method proposed in this work with a previously validated HPLC method, statistical analysis of the DPT content (as a lyophilized powder) was performed using Student's t test (p < 0.05). The percentage contents of daptomycin calculated using both methods are shown in Table V.

TABLE V Values obtained in the determination of DPT as a lyophilized powder for injectable solution, by HPLC and UV spectrophotometry 

Parameters Method
DPT content (%) 104.37 101.90 100.89 103.45 102.76 102.57
Average content (%) 102.39 102.93

a HPLC: high-performance liquid chromatography; b UV: spectrophotometry in UV region

Statistical analysis revealed that the DPT contents determined by both methods were statistically equivalent, since the tcalculated (0.51) was lower than the tcritical (2.78). Thus, these methods are interchangeable for the quantitative analysis of daptomycin in the pharmaceutical dosage form.

Although the statistical analysis demonstrated that both techniques are interchangeable, there are a number of differences between these methods to take into account when considering their advantages and disadvantages.

HPLC is one of the most commonly used techniques for the quantitative analysis of drugs in the pharmaceutical industry. This method presents some advantages, such as the ability to perform analysis in a short time, the ability to analyze complex mixtures owing to its high resolution, easy and accurate quantitative analysis, good sensitivity, and versatility, since it allows the analysis of a wide range of substances. In addition, it allows for the automation of analysis, making it convenient to conduct to routine analysis. On the other hand, one of the major disadvantages is the high cost of instrumentation and operation, since this technique requires expensive chromatographic columns and high-purity organic solvents (Collins, Braga, Bonato, 1997). Additionally, this technique uses large volumes of organic solvents for analysis, which makes it a source of occupational exposure and environmental contamination.

In contrast, UV spectrophotometry, in many cases, can be developed in an environmental-friendly way without the use of organic solvents, as demonstrated in the present work. However, even when the use of organic solvents is necessary, this technique is still advantageous when compared to HPLC, since it requires smaller amounts of organic solvents than the chromatographic method. As the UV spectrophotometry method does not require the use of costly chromatographic columns and high purity solvents, this technique is also economically advantageous. This cost advantage is even greater when the method uses water as the diluent, as it is a low cost solvent. Another advantage of this technique is the short time to conduct analysis, which makes it a practical option for routine analysis in quality control. However, one downside of UV spectrophotometry is that it is not able to detect and separate degradation products, unlike the HPLC.


In the present study, the UV spectrophotometric analytical method was properly developed, validated, and shown to be effective for the quantification of daptomycin in its pharmaceutical dosage form as a lyophilized powder for injectable solution. This method has advantages when compared to chromatographic methods, such as employing an aqueous system, rather than potentially toxic organic solvents, and it requires minimal sample preparation steps. In addition, spectrophotometric analysis uses small amounts of solvents and sample, resulting in a non-polluting method for staff and the environment.

This procedure uses simple reagents, requires minimal sample preparation, and generates only a small amount of residue. Therefore, its use is encouraged for routine analysis. The proposed method might be successfully used in the quantitative analysis of pharmaceutical formulations of daptomycin, contributing to improvements in medication quality control. In addition, a Student's t-test showed no statistically significant difference between the proposed UV spectrophotometric method and a previously validated HPLC method. Given these results, both methods are interchangeable, however the spectrophotometric method is environmentally and economically advantageous compared to the HPLC method.


This work was supported by FAPESP (São Paulo, Brazil), PADC-FCF (São Paulo, Brazil), and CNPq (Brasília, Brazil). E.G. Tótoli was funded by FAPESP (São Paulo, Brazil) and H.R.N. Salgado was funded by CNPq (Brasília, Brazil).


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Received: March 23, 2015; Accepted: July 02, 2015

*Correspondence: E. G. Tótoli. Faculdade de Ciências Farmacêuticas. Universidade Estadual Paulista "Júlio de Mesquita Filho" - UNESP. Rodovia Araraquara-Jaú, km 1, 14801-902, Araraquara, SP, Brazil. Phone: 55-16-33016967, Fax: 55-16-33016900. E-mail:

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