Int J App Pharm, Vol 10, Issue 6, 2018, 135-138Original Article


EMPLOYMENT OF ATR-FTIR AND HPLC-UV METHOD FOR DETECTION AND QUANTIFICATION OF ANDROGRAPHOLIDE

OKTAVIA INDRATI1,2, RONNY MARTIEN1, ABDUL ROHMAN3, AKHMAD KHARIS NUGROHO1*

1Department of Pharmaceutics, Faculty of Pharmacy, Universitas Gadjah Mada, Sekip Utara, Yogyakarta Indonesia 55281, 2Department of Pharmacy, Faculty of Mathematics and Natural Sciences, Universitas Islam Indonesia, Jl. Kaliurang Km 14,5 Sleman Yogyakarta Indonesia 55584, 3Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Universitas Gadjah Mada, Sekip Utara, Yogyakarta Indonesia 55281
Email: oktavia.indrati@uii.ac.id

Received: 23 Jul 2018, Revised and Accepted: 04 Sep 2018


ABSTRACT

Objective:The purpose of this present study was to describe the employment of infrared (IR) spectroscopy and high-performance liquid chromatographywith ultraviolet detection (HPLC-UV) method in determining the identity and purity of bulk material containing andrographolide.

Methods:Attenuated total reflectance(ATR)-Fourier transform infrared (FTIR) spectroscopy was carried out in transmittance mode to investigate the molecular vibration of the bulk material component and the similarity of functional groups between bulk material and standard andrographolide. Meanwhile, the liquid chromatographic analyses were performed on areversed-phase C18 column and under UV detection at 224 nm to determine the andrographolide content of the bulk material.

Results: The obtained ATR-FTIR spectra indicated that functional group of the bulk material were in close similarity with those of standard andrographolide. The linearity of the evaluated method achieved over a concentration range of 1 to 60 μg/ml with a high correlation coefficient (0.999). By using the studied HPLC-UV method, the andrographolide of bulk material was found to be 98.12% (retention time of 2.58 min).

Conclusion: The studied HPLC-UV method of andrographolide determination is accurate, precise, selective, and brief in terms of analysis time. The studiedmethod, therefore, provides a rapid and reliable assessmentforidentifying and determining the purity of andrographolide bulk material.

Keywords:Andrographolide, Bulk material, Determination, HPLC-UV, Identity, Purity


INTRODUCTION

Andrographolide (fig. 1) is a diterpenoid substance isolated from the medicinal plant of Andrographis paniculata. This compound becomesthe point of interest since A. paniculata herb is widely used as a traditional medicine in several Asian countries such as India, Indonesia, China, Malaysia, and Thailand[1,2]. A large number of studieswere conducted to isolate, identify, and quantify this substance[3–5] as well as assess its pharmacological activities[6-8], and its safety[9,10].Andrographolide is reportedtoexhibit various biological activities, including antidiabetic[11], anticancer,anti-inflammatory[6], antivirus, and hepatoprotective activities. Despite the many pharmacological activities, it is reported that andrographolide has poor aqueous solubility and is extensively metabolized leading to its low oral bioavailability[2,12]. Hence, numerous studies wereperformed to develop andrographolidecontaining dosage form in order to enhance the acceptability, solubility, and bioavailability of this bioactive compound. Numerous dosage forms such as microcrystal[13], microemulsion[14], micelle [15], nanoparticle[16], solid lipid nanoparticle [17], spray-dried [18]and suspension [19]of andrographolide have been successfully developed.

Fig.1: The chemical structure of andrographolide

The quality of the bulk material is an important factor that has to be consideredduring adosage form development process and routine analysis beforedrug manufacturing. Bulk material quality affects the quality of the finished product. Several authors have studiedthe quantification of andrographolide isolated from Andrographis paniculata herbs[3,4,20,21], but none of them reported thedetermination of andrographolide bulk material’s identity and purity.ATR-FTIR spectroscopy offers a rapid and direct analyticaltechnique without sample preparation as the advantage[22,23]. Meanwhile, HPLC-UV method is a simple and rapid technique for quantification of drug substance compared to other techniques[24], which becomes the method of choice for bulk and dosage form analysis [25-28]. Therefore, this study aims to describe the determination of andrographolide content in bulk materialemployinginfrared spectroscopy and HPLC-UV method.

MATERIALS AND METHODS

Chemical and reagents

Andrographolide bulk material was purchased from Sinobright Pharmaceutical, China while andrographolide standard (98%) was obtained from Sigma. Methanol for HPLC (J. T Baker) was used as the mobile phase.

ATR-FTIR(Attenuated total reflectance-Fourier transform infrared)

The powder of bulk material and standard andrographolide were investigated in ATR-FTIR to determine the molecular functional groups of the component and the similarity between these two samples. IR spectra were recorded by using Spectrum TwoFTIR spectrometer(Perkin Elmer,USA) with a single reflectance horizontal ATR cell. The analyses were made in transmittance mode with a small amount of sample deposited onthe ATR crystal. The transmittance was measured in the frequency range from400 cm-1 to 4000 cm-1with resolution of 4 cm-1.

Chromatographic condition

This study was conducted using Waters liquid chromatography system (e2695) that was equipped with UV detector (2486). A Sunfire C-18 column (150 x 4.6 mm, 5 µm) was used as the static phase in the chromatographic separation process. The mobile phase consisted of methanol: water (67:33) that was filtered through a 0.45 µm nylon membrane and sonicated prior to using. The flow rate of the mobile phase was set at 1 ml/min. Meanwhile, the detection wavelength was set at 224 nm. The injection volume was kept at 20 µl.Data acquisition and analyses were performed using Empower software. This chromatographic condition was adapted from a previously reported technique [3] with a slight modification in the ratio of mobile phase and also detection wavelength.

Stock solution preparation

A stock solution of andrographolide (250 μg/ml) was prepared by dissolving 12.5 mg of andrographolide standard in 50 mlmethanol. This solution was then diluted with methanol to produce a series of working standard dilution.

System suitability

Six replicate injections of bulk material containing andrographolide (30 μg/ml) were evaluated for system suitability. The evaluated parameters were retention time, tailing factor, selectivity, and resolution.

Linearity

Linearity was evaluated by injecting a series of concentrationsof andrographolide standard ranging from 1 to 60 μg/ml. Each level of andrographolide concentration was prepared in triplicate manner. A linear regression analysis was performed between the employed concentration and peak areas obtained.

Precision

Precision was evaluated in terms of repeatability and inter-day precision. Repeatabilityof the HPLC-UV method was determined by repeatedly(n = 6) injecting a solution of bulk material (30 µg/ml)and then recording the chromatogram. Meanwhile, the inter-day precisions were analysed by measuring thecorresponding responses 3 times on 3 different days for 1concentration of andrographolide (30 µg/ml). The resultswere expressed as a percentage of relative standard deviation (RSD).

Accuracy

The accuracy of the method was tested by fortifying samples (bulk material solution) with three different concentration of standard andrographolide and determining the recovery of the added standard. Three replicates of each concentration level were prepared, filtered and injected. The percentage recoveries of andrographolide were then determined.

Limit of detection(LOD) and limit of quantification(LOQ)

Limit of detection (LOD) was defined as the lowest concentration of andrographolide resulting in a signal-to-noise ratio of 3:1. Meanwhile, the limit of quantification (LOD) was expressed as a signal-to-noise ratio of 10:1. LOD and LOQof the studied method were determined by using the calibration curve data, 3.3 SD/S and 10 SD/S respectively, where SDis the standard deviation of y-intercepts and S is the slopeobtained from the calibration curve.Varied concentrations ranging from 1 to 60 μg/mlwere prepared and analysed to obtain these values.

Bulk material sample preparation

About 12.5 mg of bulk material powder was accurately weighed and dissolvedin 50 ml of methanol. The aliquotwas then taken, diluted, and filtered using a 0.45 mm membrane.It was then injected under the chromatographic condition as described earlier to determine the andrographolide content.

RESULTS AND DISCUSSION

ATR-FTIR

ATR-FTIR spectroscopy was carried out to study the similarity of thefunctional group between standard andrographolide and bulk material. The FTIR spectra ofthe bulk material showeda characteristic of lactone absorption band at 1722 cm-1, C=C band at 1674 cm-1, C-O-Cband at 1218 cm-1, and methylene at 906 cm-1 (fig.2).These absorption bands were also detected in previous studies of andrographolide IR spectra reported by other authors[20,29,30]. The obtained ATR-FTIR spectra revealed that there was a close similarity between the transmittance signals of standard andrographolide and those of bulk material. This result confirmed the identification of the bulk material as andrographolide.

Fig.2: ATR-FTIR spectra of standard andrographolide and bulk material

Wavelength selection

Andrographolide standard in methanol was scanned from 190 to 400 nm using UV-Vis spectrophotometer to assess the maximum wavelength of andrographolide absorbance. The maximum andrographolide absorbance was observedat a wavelength of 224 nm. Similar wavelength was also reported by other researchers[2]. Thus, this wavelength was selected for future analysis.

System suitability

These chromatographic conditions delivered a chromatogram having a good repeatability of peak response (standard deviation of retention time is 0.001) and low tailing factor (0.94). Theresolution between andrographolide and its nearest peakwas found to be 2.95, which was higherthan the required level (resolution/Rs>2).These parameters indicate that the system is suitable for the analysis. The results for system suitability were foundto be within the acceptable limits.

Linearity

The method presented linearity over the evaluatedconcentration rangeof1 to 60μg/mlwhich is shownby ahigh correlation coefficient (0.999). This result indicated that the linearity of the studied method complies with the regulatory requirement. The regression equation for the calibration curve was y = 38486x-7716.4, where y is the peak area and x is the concentration ofandrographolide (μg/ml). The calibration curve of series concentrations of andrographolide in methanol is shown in fig. 3.

Fig.3: Calibration curve of andrographolide in methanol

Precision, accuracy, LOD, and LOQ

The relative standard deviations for repeatability and inter-day precisions were found to be less than 2% (table 1), indicating that the studied method was precise. The overlay chromatogramobtained from precision determination is presented infig. 4.In addition, accuracywas found to be high, having a mean percentage recovery of99-101%(table 2). LOD and LOQ were found to be 1.0and3.34 μg/mlrespectively. This result indicated that themethod has proper repeatability, low inter-day variability, and accuracy in determining the andrographolide content of the bulk material. The averageretention time of andrographolide was 2.58 minunder the studied condition. This retention time was faster than that reported by a previousstudy (4.3 min) [3]. Having faster retention time can be beneficial in terms of analysis time and amount of mobile phase required for routine analysis.

Table 1: Results of a precision study of andrographolide

Parameter Mean of peak area SD RSD (%)
Repeatability* 1117621.67 10582.46 0.95
Inter-day precision** 1129007 11608.35 1.03

*result expressed in mean (n=6), **result expressed in mean (n=3), SD = standard deviation, RSD = relative standard deviation

Table 2: Results of recovery study of andrographolide

Amount of bulk material (μg/ml) Amount of andrographolide standard added (μg/ml) Amount of andrographolide found (μg/ml) Recovery±SD* (%) RSD** (%)
1 2 3
20.89 10 30.89 30.99 31.22
20.89 20 41.29 40.69 40.96
20.89 30 52.38 51.48 52.28

*result expressed in mean (n=3), SD = standard deviation, RSD = relative standard deviation

Fig.4:The overlay chromatogram of andrographolide in bulk material (n=6)

Andrographolide content determination

Despite the slight modification in the wavelength detection and proportion of mobile phase compared to previous research, the evaluated method showed a proper precision result, good accuracy, and shorter retention time. The studied method was then employed to determine the andrographolide content of the bulk material. The percentage of andrographolide inthe bulk material was found to be 98.12%.

CONCLUSION

This study demonstrated that verified HPLC-UV method of andrographolide determination is accurate, precise, selective, and short in terms of analysis time.Besides, both of ATR-FTIR spectroscopy and HPLC-UV were successfully employed in the determination of identity and purity of andrographolide in bulk material. By employing studied HPLC-UV method, the andrographolide content of bulk material was found to be 98.12%.

ACKNOWLEDGMENT

The authors are grateful to Indonesia Endowment Fund for Education (BUDI-LPDP) for providing financial support to conduct these studies.

CONFLICT OF INTERESTS

Declared none

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About this article

Title

EMPLOYMENT OF ATR-FTIR AND HPLC-UV METHOD FOR DETECTION AND QUANTIFICATION OF ANDROGRAPHOLIDE

Keywords

Andrographolide, Bulk material, Determination, HPLC-UV, Identity, Purity

DOI

10.22159/ijap.2018v10i6.28691

Date

22-11-2018

Additional Links

Manuscript Submission

Journal

International Journal of Applied Pharmaceutics
Vol 10, Issue 6 (Nov-Dec), 2018 Page: 135-138

Online ISSN

0975-7058

Authors & Affiliations

Oktavia Indrati
Department of Pharmaceutics, Faculty of Pharmacy, Universitas Gadjah Mada Sekip Utara, Yogyakarta Indonesia 55281 Department of Pharmacy, Faculty of Mathematics and Natural Sciences, Universitas Islam Indonesia Jl. Kaliurang Km 14,5 Sleman Yogyakarta Indonesia 55584
Indonesia

Ronny Martien
Department of Pharmaceutics, Faculty of Pharmacy, Universitas Gadjah Mada Sekip Utara, Yogyakarta Indonesia 55281

Abdul Rohman
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Universitas Gadjah Mada Sekip Utara, Yogyakarta Indonesia 55281
Indonesia

Akhmad Kharis Nugroho
Department of Pharmaceutics, Faculty of Pharmacy, Universitas Gadjah Mada Sekip Utara, Yogyakarta Indonesia 55281
Indonesia


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