Method development for acetyl octapeptide-3 analysis by liquid chromatography-tandem mass spectrometry

Abstract

Background

Acetyl octapeptide-3 (SNAP-8) is an antiaging peptide that is more effective than acetyl hexapeptide-3, which is more stable than botulinum toxin and effectively relieves facial wrinkles. Products containing SNAP-8 such as patch are producing, but analytical method has not been reported to determination of SNAP-8.

Method

Mobile phase, collision energy, and desolvation line temperature were optimized, and mass spectral data set for SNAP-8 was newly constructed by liquid chromatography-triple quadrupole mass spectrometer in multiple reaction monitoring mode.

Results

The developed method showed good linearity (r ≥ 0.9971) with limit of quantification of 0.0125 ng/mL, repeatability (% relative standard deviation = 0.02 to 0.12) and accuracy (% relative error = − 1.68 to 1.44) under optimal conditions. This method was successfully applied to a biodegradable microneedle patch loaded with SNAP-8.

Conclusion

The present method for the quantification of SNAP-8 may be useful for quality control in the cosmetic fields.

Introduction

The synaptosome-associated protein of 25 kDa (SNAP-25) is known to relate to facial wrinkles including muscle contraction (Adler et al. 2001). The acetyl hexapeptide-3 is a peptide fragment of SNAP-25 and it has been widely used for the cosmetic materials of the improvement of facial wrinkles because acetyl hexapeptide has an inhibiting effect on the function of SNAP-25 (Lipotec™). An acetyl octapeptide-3 (SNAP-8) added a two-amino acid chain on acetyl hexapeptide-3, which was designed for better effect of wrinkle improvement than acetyl hexapeptide-3 (Lipotec™). A botulinum toxin (BOTOX®) has been widely used for the improvement of facial wrinkles, but SNAP-8 has higher safety than BOTOX® (Blanes-Mira et al. 2002; Zhou et al. 2011). Both SNAP-8 and a botulinum toxin (BOTOX®) target the SNAP-25. BOTOX® breaks the SNAP-25 and causes muscle paralysis, while SNAP-8 captures the SNAP-25 and causes muscle relaxation (Blasi et al. 1993; Gutiérrez et al. 1995; Gutierrez et al. 1997; Blanes-Mira et al. 2002; Yamauchi and Lowe 2004). Thus, SNAP-8 is more stable than BOTOX®, which has been proposed as a functional cosmetic material that can replace BOTOX® (Lipotec™; Blanes-Mira et al. 2002). Although SNAP-8 is being used in functional cosmetics, method for SNAP-8 analysis has not been reported. Patches are generally used as an example of skin delivery products. Polymeric compounds such as peptides cannot pass through the stratum corneum and skin absorption is also difficult (Park et al. 2005). However, microneedle patches penetrate the dermal layer and can transfer substances such as SNAP-8 with large molecular weights directly into skin, which were used for the transdermal delivery of polymeric compounds (Zhang et al. 2014). In this study, analytical method of SNAP-8 was developed by liquid chromatography-tandem mass spectrometry (LC-MS/MS). This method was successfully applied to quantification of SNAP-8 level in biodegradable microneedle patches.

Materials and methods

Materials

SNAP-8 and the acetyl hexapeptide-3 as internal standard (IS) were purchased from Lipotec (Barcelona, Spain); their chemical structures are shown in Fig. 1. Biodegradable microneedle patches containing SNAP-8 were provided by Raphas Co. Ltd. (Seoul, Republic of Korea). High-performance liquid chromatography (HPLC) grade water and acetonitrile (ACN) were purchased from Daejung Chemical (Siheung-si, Gyeonggi-do, Republic of Korea). The syringe-driven filter unit (0.45 μm) was purchased from Merck Millipore (Darmstadt, Germany). Formic acid (FA) and trimethylamine (TEA) were purchased from Wako Pure Chemical (Richmond, VA, USA). All other chemicals were of analytical reagent grade.

Fig. 1

Chemical structures of SNAP-8 and IS

Preparation of standard and calibration solutions

Stock solutions of SNAP-8 and IS were made up at 10.0 μg/μL in HPLC grade water. Working standard solutions were prepared by diluting each stock solution to 12.5 ng/μL (SNAP-8) and 15.0 ng/μL (IS), respectively. The SNAP-8 standards for quantitative calibration curve were prepared from 0.0125 to 0.15 ng/μL by aliquots of each working standard solution. All standard solutions were then stored at 4 °C.

Preparation of microneedle patches

Biodegradable microneedle of patch (1.42 mg) with loaded SNAP-8 was extracted with distilled water (5 mL) containing IS (150.0 ng). The extract was filtered with syringe-driven filter unit (0.45 μm), then an aliquot of 10 μL was injected into the LC-MS/MS system.

Method validation for SNAP-8 analysis

Linearity, repeatability, accuracy, recovery, limit of detection (LOD), and limit of quantification (LOQ) were validated under optimal conditions with blank patch matrix. Calibration dynamic range was performed from 0.0125 to 0.15 ng/μL. Slope, intercept, and correlation coefficient (r) were determined by using the least-squares regression analysis form the calibration curve constructed based on relative peak area ratios to IS. LOD was evaluated by injection following dilution with standard solution at the minimum concentration of calibration range. LOQ of SNAP-8 was defined as minimum concentration in the calibration range. The repeatability as relative standard deviation (%RSD) and the accuracy as relative error (%RE) were obtained from two different concentrations from triplicate experiments under the optimal conditions. The recovery was evaluated by comparing the percentages of peak area ratio of filtered to that of non-filtered sample (recovery of 100%) including same concentration of SNAP-8.

Liquid chromatography-tandem mass spectrometry

LC-MS/MS analysis was performed in multiple reaction monitoring (MRM) mode using a Shimadzu Nexera UPLC system (Shimadzu Corp., Kyoto, Japan) coupled with a LCMS-8050 triple quadrupole mass spectrometer (Shimadzu Corp., Kyoto, Japan) equipped with an electrospray ionization (ESI) interface in positive ionization mode. Chromatographic separation was performed using a betabasic-18 column (30 mm × 2.1 mm, 5 μm, 150 Å, Thermo Electron, Waltham, MA) equipped with a betabasic-18 guard column (10 mm × 2.1 mm, 5 μm, 150 Å, Thermo Electron, Waltham, MA), which separates polar peptides like SNAP-8 in reverse phase mode. The column oven was maintained at 40 °C and the autosampler temperature at 4 °C. Gradient elution was performed using solvent A (HPLC grade water containing 0.1% FA) and solvent B (ACN containing 0.1% FA) in total flow rate of 0.3 mL/min. Gradient condition of solvent B was initiated from 0% (0.5 min) and was increased up to 40% (0.5 to 5 min), and then held for 1 min (5 to 6 min), and then return to the initial condition for the next run and hold for 2 min (6 to 8 min). An aliquot 10 μL of each sample was injected into the LC-MS/MS system. The mass spectrometer interface temperature was maintained at 200 °C, the nebulizing gas flow was at 3.0 L/min, desolvation line (DL) temperature at 200 °C, and heat block temperature at 400 °C. The pressure of collision-induced dissociation (CID) gas was at 270 kPa. SNAP-8 and IS were successfully detected in the product-ion scan mode. Quantitative analyses were performed in the MRM transition mode with quadrupole 1 (Q1) and quadrupole 3 (Q3) operated at unit resolution. A dwell time and pause time were set at 22.0 ms for selected ions.

Result and discussion

Optimal conditions for SNAP-8 analysis by LC-MRM-MS/MS

The effects of FA and TEA as additives in the mobile phase were investigated. In this result, FA was used due to higher intensity (about six times) than those of TEA (Table 1). A C₁₈-column (5 μm, 150 Å) with equipped a guard column was selected for peptide analysis. Analysis of SNAP-8 was performed using gradient elution within 2 min. The precursor ions of SNAP-8 and IS were selected with each multiply charged ion in ESI mode. The [M + 2H]²⁺ ions of SNAP-8 (m/z 538) and IS (m/z 445) were selected as precursor multiple ions in positive mode. The [M + H]⁺ ions of SNAP-8 (m/z 1076) and IS (m/z 890) were detected at low intensities and the [M + 3H]³⁺ of SNAP-8 was not detected. The intensity of SNAP-8 was monitored with the desolvation line (DL) temperature from a range of 200 to 275 °C. DL temperature was optimized for [M + 2H]²⁺ intensity at 200 °C (Fig. 2). Q3 SCAN spectra of SNAP-8 (a) and IS (b) are shown in Fig. 3. Precursor ions of SNAP-8 (m/z 538) and IS (m/z 445) were fragmented with collision energy, both product ions of SNAP-8 and IS were optimized to m/z 102, 84, and 144, respectively. Optimal collision energies were monitored for SNAP-8 (m/z 102 (− 30 V), m/z 84 (− 48 V), and m/z 144 (− 25 V)) and IS (m/z 102 (− 39 V), m/z 84 (− 55 V), and m/z 144 (− 30 V)). Optimized MRM conditions are summarized in Table 2 and MRM chromatograms of SNAP-8 and IS are shown in Fig. 4.

Table 1 Comparison of ionic strength between TFA and FA as additives in the mobile phase

Fig. 2

Optimization of DL temperature in the range 200 to 275 °C

Fig. 3

Mass spectral patterns of SNAP-8 (a) and the IS (b) by LC-MS/MS with ESI mode

Table 2 Ion transitions and collision energy values of SNAP-8 and IS

Fig. 4

MRM chromatograms of the blank spiked with IS (a) and SNAP-8 and IS (b) by LC-MS/MS

Method validation for SNAP-8 analysis by LC-MS/MS

SNAP-8 was detected as a single peak at 1.7 min in extracts of a blank patch spiked with SNAP-8 standard. Chromatograms of SNAP-8 in extracts of blank patch spiked with IS (a), and extracts of blank patch spiked with SNAP-8 and IS (b) are shown in Fig. 4. The good linearity was obtained with correlation coefficient (r) of 0.9971 in the range from 0.0125 to 0.1250 ng/mg. LOD and LOQ were evaluated with diluted standard solution and their levels were 0.0025 and 0.0125 ng/mg, respectively. Repeatability of 0.05 and 0.1 ng/mg showed 0.20 and 0.02 (%RSD), respectively. Accuracy were 1.44 and − 1.68 (%RE) at 0.05 and 0.1 ng/mg, respectively. The recovery showed 76.7% at 0.125 ng/mg of microneedle of patch (Table 3). In the stability test, SNAP-8 was stable at least 96 h when this was refrigerated at 4 °C (Table 4 and Fig. 5). Therefore, this method was suitable for quantification and evaluation test of SNAP in patch products.

Table 3 Validation data set of SNAP-8 by LC-MS/MS

Table 4 Stability test of SNAP-8 in DW at 4 °C

Fig. 5

Stability test of SNAP-8 for 96 h at 4 °C

Patch matrix effects for SNAP-8 analysis

Two different calibration curves were compared to assess matrix effects for measurements made using blank patches or HPLC grade water, and SNAP-8 in microneedle patches were quantified. Based on the results of four patches, the calculated SNAP-8 level using HPLC grade water calibration curve was 89.5 ± 10.5 ng, while it was 76.9 ± 8.6 ng by using matrix calibration curve including blank patches. In this result, the calculated SNAP-8 level using matrix calibration curve was 16.3% smaller than HPLC grade water-based values. Therefore, the matrix effects of patches must be considered for quantitative analysis of SANP-8.

Conclusion

Analytical method of SNAP-8 was developed by LC-MS/MS in MRM mode. In the optimal condition, linearity (r ≥ 0.9971), repeatability (%RSD = 0.02 to 0.12), accuracy (%RE = − 1.68 to 1.44), and recovery (76.7%) showed with LOD of 0.0025 ng/mg and LOQ of 0.0125 ng/mg. When applied to patch product, SNAP-8 was identified and determined as 76.9 ± 8.6 ng. Therefore, this method was suitable for determination of SNAP-8 in patch products, which will be useful for quality control and evaluation test of SNAP-8 in the cosmetic fields.