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Development and Validation of A Liquid Chromatography Method For The Analysis of Paromomycin Sulfate and Its Impurities 2155 9872.1000102
Development and Validation of A Liquid Chromatography Method For The Analysis of Paromomycin Sulfate and Its Impurities 2155 9872.1000102
Abstract
A rapid and simple method for the separation and quantification of paromomycin sulfate and its impurities by
HPLC coupled with evaporative light scattering detection (ELSD) was developed. The chromatographic conditions
included the use of a GRACE Alltima C18 column (250mm×4.6mm, 5μm) maintained at 30°C and a mobile phase of
0.2 M trifluoroacetic acid water–acetonitrile (96:4, v/v) at a flow rate of 0.6 mL/min. The influence of gas pressure and
temperature of the drift tube in the detector on the detection response was also investigated. A system suitability test to
check the quality of the separation was specified. The method showed good repeatability, linearity and robustness. It
also enabled the simultaneous determination of the inorganic counter ions (sulfates).
Keywords: Paromomycin sulfate; Impurity; HPLC; ELSD low detection limits for aminoglycoside antibiotics [15]. Like other
aminoglycosides, paromomycin has no ultraviolet (UV) absorbing
Introduction chromophores, and therefore the derivatization of the amino groups
Paromomycin (PARO, synonym: aminosidine, Figure 1), a broad is required for high-performance liquid chromatography (HPLC)
spectrum aminoglycoside antibiotic first isolated in 1956 from the analyses with UV detection [16]. A HPLC method with fluorescence
fermentation of streptomyces[1], shows activity against both gram- detection is also developed with post-column derivatization with
positive and gram-negative bacteria as well as some protozoa ortho-phthalaldehyde (OPA) and 2-mercaptoethanol. Pre-column
and cestodes. Although it is not used as an antibiotic any more, labeling with OPA is not used because of the low stability of the
paromomycin has been approved since 2007 in India as an effective, derivative [17]. Because of the thermal instability of aminoglycosides,
well tolerated and affordable treatment for visceral leishmaniasis (VL) the analysis of aminoglycosides by GC or gas-chromatography/mass
[2]. Recently it is being developed for use against multi-drug resistant spectrometry (GC/MS) is difficult [18]. The analysis of paromomycin
strains of tuberculosis [3-4] and for the treatment of intestinal by evaporative light-scattering detection (ELSD) has not been
cryptosporidiosis in AIDS patients [5-8]. reported previously. ELSD has been applied as a universal detection
method [19,20] when coupled with liquid chromatography. Different
Various methods have been developed for the analysis of
aminoglycosides generally produce the same response with ELSD
paromomycin, which include capillary zone electrophoresis [9]
detection. Therefore, the impurities can be easily quantified [21].
, capillary electrophoresis [10] , reverse-phase ion-pairing HPLC
The present study developed and validated a specific, accurate and
coupled with pulsed amperometric detection [11], LC-MS[12,13],
relative sensitive HPLC-ELSD method for determining paromomycin
the use of silver-coated gold nanoparticles as concentrating probes
sulfate and its impurities. This method also enables the simultaneous
and matrices for surface-assisted laser desorption/ionization mass
determination of the inorganic counter ions (sulfates).
spectrometry [14], and gas-liquid chromatography. Aminoglycosides
can be oxidized and therefore directly detected by amperometry. Experimental
Pulsed amperometric detection (PAD) has broad linear range and very
Reagents and samples
HPLC grade trifluoroacetic acid (TFA) was purchased from Tedia
(America). HPLC grade methanol and acetonitrile were purchased from
Merck (Darmstadt, Germany). Paromomycin RS (batch no. 130371-
200305) and Neamine RS (Batch No. 85-1106) were purchased from
the National Institute for the Control of Pharmaceutical and Biological
Products, China. Paromomycin samples (Batch No. 20050409-004,
*Corresponding author: Ying Liu, Henan Provincial Institute for Food and Drug
Control, Zhengzhou, China, Tel: 0086037163388265; Fax: 0086037163388265;
E-mail: [email protected]
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Paromomycin is a mixture of two isomers whose ratios vary with indirect UV detection coupled with micellar electrokinetic capillary
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and toxicity. For example, the toxicity and the side effect of L and
11. Pastore P, Gallina A, Magno F (2000) Description and validation of an analytical
D neamine are different [27]. Paromomycin has paromomycin method for the determination of paromomycin sulfate in medicated animal
and isomers. Paromomycin is produced by fermentation, and the feeds. Analyst 125: 1955-1958.
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antibacillus subtilis activity of paromomycin [28], and therefore 13. Rona K, Klausz G, Keller E, Szakay M, Laczay P, et al. (2009) Determination
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as concentrating probes and matrices for surface-assisted laser desorption/
components. The related substances also could be controlled by this ionization mass spectrometric analysis of aminoglycosides. J Am Soc Mass
method, and further study is needed. Spectrom 20:1925-1932.
We also used the Alltech 2000 ELSD, a high temperature 15. Szunyog J, Adams E, Roets E, Hoogmartens J (2000) Analysis of tobramycin
by liquid chromatography with pulsed electrochemical detection. J Pharm
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16. Lu J, Cwik M, Kanyok T (1997) Determination of paromomycin in human
were also studied. The shift tube temperature was 100°C and the gas plasma and urine by reversed-phase high-performance liquid chromatography
flow rate was 2.4 L/min. The Alltech 2000 ELSD has a better LOD than using 2,4-dinitrofluoro benzene derivatization. J Chromatogr B Biomed Sci Appl
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Therefore, it is better to determine the related substances by using 17. Soltes L, Sebille B (1999) A simple chiral high-performance liquid
a high temperature evaporative light scattering detector such as chromatographic method to study the enantiomer-differentiating action of
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Acknowledgements 18. Kennedy DG, McCracken RJ, Cannavan A, Hewitt SA (1998) Use of liquid
Funded by the National Key New Drug R&D Program Foundation of China chromatography–mass spectrometry in the analysis of residues of antibiotics
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