Int J App Pharm, Vol 11, Issue 5, 2019, 313-316Original Article


THE EFFECT OF THERMAL STERILIZATION AND EXCIPIENTS ON THE STABILITY OF ASCORBIC ACID IN AQUEOUS SOLUTIONS

A. V. SYROESHKIN1, T. V. PLETENEVA1*, E. V. USPENSKAYA1, O. V. LEVITSKAYA1, S. S. BARSEGYAN2, I. A. ZLATSKY1, M. A. TRIBOT-LASPIERE1

1Peoples Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation, 2Russian Center for Forensic Medicine, 12/13 Polikarpova St, Moscow, 125284, Russian Federation
Email: tvplet@mail.ru

Received: 10 May 2019, Revised and Accepted: 06 Aug 2019

ABSTRACT

Objective: To investigate the thermal stability of aqueous solutions of L-ascorbic acid (AA) and its reactions with excipients for the improvement of the injection forms technology.

Methods: Solutions of L-ascorbic acid were prepared using deuterium depleted water (DDW-«light» water, D/H=4 ppm) and natural deionized high-ohmic water (BD, D/H=140 ppm). The optical rotation was observed using an automatic polarimeter Atago POL-1/2. Electrospray tandem mass spectra were recorded by Sciex X500R QTOF. Electronic spectra were recorded by UV-spectrometer Cary 60 (Agilent). Unicellular biosensor (Spirotox-test) was used for investigation of excipients influence on the AA biological activity. The statistical analysis was carried out using the OriginPro®9 packages.

Results: The results demonstrate the thermal instability of AA. The optical activity of injection forms of AA differs from model solutions with the same concentration and pH value but without heat treatment. Monitoring of solutions by the LC-ESI-MS/MS method made it possible to characterize the nature of some thermal decomposition products. Thermodynamic calculations and evaluation of biological activity (Spirotox-test) indicate that AA interacts with sulfite-ion by redox mechanisms. Excipients in AA aqueous solutions decrease, but DDW increases the biological object lifetime.

Conclusion: The use of the set of physicochemical and biological methods to study the effect of heat treatment of L-ascorbic acid solutions in the presence of sulfur (IV) compounds as excipients made it possible to identify decomposition products of the active pharmaceutical ingredient. The results indicate the need to exclude sterilization of the AA injection form by the thermal method and replace it with an alternative one, for example, with gamma radiation treatment.

Keywords: L-Ascorbic acid, Heat sterilization, Sulfur (IV) excipients, Polarimetry, Electron spectrometry, Electrospray tandem mass spectrometry, Spirotox-test

© 2019 The Authors. Published by Innovare Academic Sciences Pvt Ltd. This is an open-access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
DOI: http://dx.doi.org/10.22159/ijap.2019v11i5.34025

INTRODUCTION

Since the middle of the last century, the stability of ascorbic acid (AA), which has antioxidant properties in mammals and in foodstuffs, has been actively studied [1-9]. AA degradation can occur spontaneously, even in an anaerobic environment, and under the influence of a number of factors [1, 2, 5]. An increase in temperature and in alkalinity of its solution, exposure to radiation, the presence of d-elements ions and compounds with a more positive redox potential are the main causes of AА degradation.

To increase the stability of AA, sodium sulfite (Na2SO3) or its analogues with sulfur (IV) in anionic form — sodium hydrogen sulfite/bisulfite (NaHSO3) or sodium metabisulfite/pyrosulfite (Na2S2O5) — are added to liquid dosage forms. At the same time, the possibility of AA interaction with these excipients, which exhibit oxidative properties with respect to vitamin C, is ignored [10, 11]. Redox reactions are accompanied by an increase in impurities in the liquid dosage form. The nature of these compounds can vary depending on the acidity of the medium. The approximation to the pH of biological media increases the instability of AA and, therefore, the number of products of interaction with excipients.

In accordance with the technological regulations, sterilization of AA injection forms is performed at 100 °С (15 min) or 120 °С (8 min) [12-14], although the recommended temperature range for storing the finished injection form is between 2 °C to 8 °C [15, 16]. To justify the inadmissibility of thermal sterilization of injectable forms of AA, it is possible to use the polarimetry method: the optical activity of injectable forms of AA should differ from model solutions with the same pH and concentration values but without heating. Additional monitoring of model solutions by LC-ESI-MS/MS can characterize the nature of the products of thermal decomposition of AA. Thermodynamic calculations, polarimetric measurements and evaluation of biological activity (Spirotox test) can demonstrate that AA and sulfite ion interact through redox mechanisms.

The introduction of sulfur (IV) compounds as reducing agents in the AA injection forms and their subsequent thermal sterilization should be excluded since they are accompanied by contamination of the pharmaceutical product.

The investigation of the thermal stability of ascorbic acid in aqueous solutions and its reactions with excipients will help to improve the technology for producing injection forms.

MATERIALS AND METHODS

Materials

L-threo-Ascorbic acid was obtained from Sigma-Aldrich (the content of API ≥99%). Deionized high-ionic water (specific electrical resistivity of 18.2 MΩ×cm at 25 °C) was prepared by purifying a pyrogenic distilled water (BD, D/H = 140 ppm) on a Milli-Q system (Millipore, Great Britain). Water with low deuterium content (deuterium depleted water-DDW, D/H = 4 ppm, “light” water) was obtained by low-temperature vacuum distillation. Methanol HPLC grade, acetonitrile (Merck, hyper grade for LC-MS), ammonium formate (for HPLC, ≥99.0%, Fluka Sigma-Aldrich), deionized water for HPLC were used in experiment.

The injectable forms of vitamin of different manufacturers contained: 5.000 g AA, 0.200 g Na2SO3, 2.385 g NaHCO3, distilled water to 100 ml (pH 6.3). Model solutions (5% AA) were prepared by dissolving 5 g AA in 100 ml of BD or DDW and adding excipients at pH 6.3.

Methods

The optical activity was determined using the Atago POL-1/2 polarimeter (Japan), in the 100 mm cell, the measurement accuracy of±0.002 ° and the resolution of 0.0001 °. The electronic Peltier module was used for setting the required temperature (T=20 °C). UV spectra were recorded using an Agilent Cary 60 Spectrometer.

Liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS) was used for monitoring AA degradation. Chromatographic separation of the mixture of compounds was carried out under the following conditions: in a gradient mode (Kinetex column C18 from Phenomenex); the eluent flow rate 0.4 ml/min; the column temperature 40 °C; the volume of injected sample 10 μL. The mobile phase consisted of solution A (0.01 M solution of ammonium formate) and solution B (methanol-acetonitrile 50:50). High-resolution mass spectra were obtained using Sciex X500R Q-TOF mass spectrometer with a Turbo V™ ionization source. The mass spectrometer was operated in the negative electrospray ionization (ESI) mode. High-resolution mass spectra were obtained in the mass range 10-1000 Da. Mass fragmentation was carried out in collision energy (CE) of 35 V and collision energy spread (CES) in the interval±15 V. The voltage of the ionization source was 2500 V at 600 °C. Unicellular biosensor based on free-living ciliate Spirostomum ambiguum (the class Heterotrichea)-Spirotox-test.

Statistics

The findings were processed by the statistical methods using software packages of Origin Pro 9.1. Each value on the fig. represents «mean±SD», *P<0.05.

RESULTS AND DISCUSSION

The AA degradation kinetics was investigated at 90 °C and pH 6.3 (phosphate buffer solution). In 45, 90, 135 and 180 min after the heating start the optical rotation angle and the absorption maximum at λ=256 nm of 5 solutions, including the original, were detected at 20 °C (fig. 1).

As can be seen from the obtained results, the thermal degradation of AA does not follow the steady-state kinetics mechanism, and each experimental point is characterized by a significant amount of relative standard deviation. In the time interval 50–100 min, an absorption increase is observed. This is the result of the intermediate degradation product formation that absorbs light at 265 nm. With longer heating, the absorption of the solutions decreases as a result of the degradation of both AA and intermediate decomposition products.

Fig. 1: Kinetics of L-ascorbic acid degradation at 90 °C: a) the values of the angle of the polarized light plane rotation (α), C = 0.2%, T = 20 °C. b) Absorption at 265 nm (A), C = 0.002%. n = 5, P = 0.95

Chromatographic analysis of solutions with different thermal exposure periods indicates a decrease in the peaks of AA and dehydroascorbic acid (DGAA) in 45 min after the heating start (fig. 2). After 90 min there are many chromatographic peaks corresponding to the decay products. After 180 min of dissolution, they were not detected in either ascorbic or dehydroascorbic acids.

A

B

C

Fig. 2: HPLC chromatograms of ascorbic acid solution (pH=6,6) heated at 90 °C for 0 (a), 45 (b), 90 (c) min

Some of the degradation products were identified by liquid chromatography-electrospray ionization-tandem mass spectrometry (Fig.3). Among the identified compounds there are derivatives with m/Z: 55–2-propyn-1-ol; 59–(E)-1,2-ethenediol or acetic acid; 71–3-hydroxypropen-1-al; 89–(1Z)-1-propene-1,2,3-triol or 2,3-dihydroxypropanal; 99–1-keto-buta-1,3-diene-2,4-diol 143–5-(hydroxymethyl)-2,3,4(5H)-furantrione; 173–dehydroascorbic acid or 5-(1,2-dihydroxyethyl)-2,3,4(5H)-furantrion.

The results demonstrate the thermal instability of AA, and the formation of numerous decomposition products does not obey the laws of stationary kinetics. That´s why FDA believes that AA solutions after heat treatment are not safe; therefore low doses of gamma radiation should be used to sterilize injectable forms of vitamins, including ascorbic acid [16-18].

Fig. 3: Some derivatives of ascorbic acid in its solution heated at 90 °C for 135 min by LC-ESI-MS/MS. Identified compounds are marked in red

The presence of Na2SO3 in the injection form exacerbates the situation, since when heated, in addition to the hydrolysis products and pH increasing, the redox interaction between the SO32-ions and AA is possible. In these reactions, sodium sulfite loses its function as an excipient and plays the role of an oxidizing agent rather than a reducing agent with respect to AA. This can be demonstrated by the example of one of the possible reactions:

AA and DHAA

Electromotive force (EMF) of this process ∆E ° = E °(Ox)-E °(Red) = E °(SO32-/S2O32-)-E °(DHAA/AA) = 0.608 V, and Gibbs energy ∆Gо =-n•F•∆E ° =-234.7 kJ/mol. This value is many times greater than the values of the Gibbs energy for the state of chemical equilibrium (±10 kJ/mol) [19]. Thus, on the basis of thermodynamic calculations, the possibility of the interaction of AA as a reducing agent with compounds of sulfur in an intermediate oxidation state (+4) can be demonstrated.

The effect of disodium sulfite on the biological activity of AA was demonstrated on the Spirostomum ambigua biosensor (fig. 4). The D/H ratio decrease in water leads to an increase in the lifetime of the ciliate due to the manifestation of the kinetic isotope effect [20-22]. But any complication of the system due to the addition of excipients to the aqueous solution leads to a decrease in lifetime leads of the biological object. At the same time, there is also a noticeable increase in the specific optical rotation, which reflects a change in the chiral properties of the API solution [1, 2].

Fig. 4: The lifetime of the bilogical sensor (a) and specific rotation value (b) for laboratory model samples with different composition (1-4) and industrial injection form (5): 1-ascorbic acid (5 %); 2-ascorbic acid+NaHCO3; 3-ascorbic acid+Na2SO3; 4-ascorbic acid+Na2SO3+NaHCO3; (pH=6,30, n=3, P=0,95). The inset shows a plot of Spirostomum ambigua lifetime in Na2SO3 solutions with different ratios of D/H in water: A–140 ppm; B–4 ppm (n=5, Р=0,95)

The search for methods to protect AA drugs from degradation is not an easy task [15, 18, 21, 22] and requires an approach using a complex of analytical and biological methods [1, 6-9, 20, 23, 24]. This is especially important for injectable forms of AA [25]. The article results indicate that heating solutions of ascorbic acid and the use of sulfur compounds in the oxidation state +4 as excipients are accompanied by changes in their physical properties and chemical composition. This should be taken into account in the pharmaceutical production of injectable forms of AA and also in food production.

CONCLUSION

The use of the set of physicochemical and biological methods to study the effect of heat treatment of L-ascorbic acid solutions in the presence of sulfur (IV) compounds as excipients made it possible to identify decomposition products of the active pharmaceutical ingredient. The results indicate the need to exclude sterilization of the AA injection form by the thermal method and replace it with an alternative one, for example, with gamma radiation treatment.

ACKNOWLEDGMENT

The publication has been prepared with the support of the «RUDN University Program 5-100».

AUTHORS CONTRIBUTIONS

All the authors have contributed equally

CONFLICT OF INTERESTS

Declared none

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