Analysis of Fast Moving Consumer Goods (FMCG) using GCMS with static and dynamic headspace (HS)

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PO-CON1789E Analysis of Fast Moving Consumer Goods (FMCG) using GCMS with static and dynamic headspace (HS) ASMS 2017 TP 280 Dheeraj Handique, Ankush Bhone, Durvesh Sawant, Prashant Hase, Sanket Chiplunkar, Nitish Suryawanshi, Ajit Datar, Jitendra Kelkar and Pratap Rasam Shimadzu Analytical (India) Pvt. Ltd., 1 A/B Rushabh Chambers, Makwana Road, Marol, Andheri (E), Mumbai-40009, Maharashtra, India.

Introduction Accurate screening, characterization and quantitative analysis of flavour & fragrance (F & F) components is essential for FMCG industries and subsequent reverse engineering, especially when unknown finished good to be analysed is in solid form. Conventional methods of GC analysis often lead to qualitative results and are time consuming and troublesome with regards to sample preparation techniques. In this analysis, neat consumer products (Figure 1) were analysed directly in HS sampler, applying different analytical techniques like static and dynamic headspace and their results were compared. In both the headspace technique it requires minimal sample preparation that significantly reduces overall analysis time without sacrifice in quality data. F & F components were determined at trace levels by Shimadzu GCMS-QP2010 Ultra with HS-20 system. Figure 1. Consumer products Method of Analysis Extraction of F & F from consumer sample Commercially available consumer products like soap, shower gel, tooth paste, body lotion and orange juice were purchased from local market. Static () and Dynamic () headspace techniques were employed for qualitative analysis. For sample preparation (Figure 2), individual products were weighed in HS vial and crimped immediately using Aluminium cap with PTFE/ Silicon septum. 2

Soap, Mouth Freshener, Shower Gel & Orange Juice 20 mg 40 mg µl 20 ml Figure 2. Representation of sample preparation for HS analysis technique employed single extraction of sample in static mode whereas dynamic technique used multiple extractions to concentrate sample in trap, which were further analysed by GC-MS. Figure. GCMS-QP2010 Ultra coupled with HS-20 System by Shimadzu HSGC-MS Analytical conditions The instrument configuration used is shown in Figure. Samples were analyzed using HS-20 coupled with GCMS-QP2010 Ultra as per below conditions as shown in Table 1.

Headspace Parameters Table 1. Analytical conditions Mode : Oven Temp. (Juice sample) : C (80 C) Sample Line Temp. : 10 C Transfer Line Temp. : 180 C Cooling Temp. : NA Desorb Temp. : NA Equilib. Temp. : NA Multi Injection Count : 1 Pressurizing Gas Pressure : 10 kpa Equilibrating Time : 0.0 min Pressurizing Time : 1.0 min Load Time : 0.0 min Injection Time : 1.0 min Needle Flush Time : 4.0 min GC Cycle Time :.0 min C (80 C) 10 C 180 C -20 C 00 C -10 C 10 kpa 0.0 min 1.0 min 0.0 min 10.0 min 4.0 min.0 min Chromatographic Parameters Column : Rxi-Sil MS (0 m L x 0.2 mm ID x 0.2 μm) Injection Mode : Split Split Ratio : (.0 for Juice sample) Carrier Gas : Helium Flow Control Mode : Linear Velocity Linear Velocity : 6. cm/sec Pressure :.6 kpa Column Flow : ml/min Total Run Time : 4.0 min Column Oven Temp : Rate C/min Temperature C Hold time (min) ----.0 0.0 20.0 0.0.0 Mass Spectrometry Parameters Ion Source Temp : 200 C Interface Temp : 20 C Ionization Mode : EI Event Time : 0.0 sec Mode : Scan Start m/z : 40 End m/z : 400 4

Results Sample analysis using HS and technique Same amount of samples of different products were analyzed on HSGC-MS loop and trap mode to compare the sensitivity. Difference in number of peaks and their comparative areas using two techniques are shown in Table 2 and respectively. The chromatograms are shown in figure 4. Table 2. Comparative result of and mode analysis Summary of Comparison Between and for Different Products Sr. No. Product Vial Temp C Split Ratio HS Mode HS Mode 1 80 28 2 66 18 Mouth Freshner 6 17 4 Shower Gel 86 16 82 6 Soap 8 107 Table. Area comparison from and Mode for Major Components in Different Products Sr. No. Product Components Area (x) Area Increased Area in Limonene 10291 189804 4x 1 Pentane, 2,2,4-trimethyl- 2720 6702 1x Terpineol <alpha-> 988 278269 46x Menthol 26911667 469422497 17x 2 Camphor 29602 47964646 1x Eugenol 2106209 91114898 19x Menthol 24864908 48818291 20x Mouth Freshner Propylene Glycol 280626 22696 80x Terpinyl acetate 4796880 2214417 46x Benzeneethanol 04791 770006 1x 4 Shower Gel Linalool 6080 68041272 12x Acetic acid, phenylmethyl ester 4480261 2020 12x Phenoxyethanol 1287788 17679640 14x Isopropyl palmitate 889082 1791601 1x Heptadecanol <n-> 29861 6721676 2x Dihydromyrcenol 29778 4890270 16x 6 Soap Cyclohexanol <2-tert-butyl-, trans-> acetate 196812 9086 20x Linalyl acetate 762749 491696 16x

Table 4. Reproducibility data for Limonene from orange juice in mode Sr. No. Product Component % RSD (n=6) 1 Limonene 7.0 2.0 2.2 2.00 1.7 1.0 1.2 0.7 0.0 0.2 0.0.0 10.0 1.0 20.0 2.0 0.0.0 40.0 Shower Gel 2.2 2.00 1.7 1.0 1.2 0.7 0.0 0.2 0.0.0 10.0 1.0 20.0 2.0 0.0.0 40.0 7.0 2.0 6.0 2.2.0 4.0 2.00 1.7 1.0.0 1.2 2.0 1.0 0.0 0.7 0.0 0.2 10 20 0 40 10 20 0 40 Mouth Freshener Soap 6.0 1.7 1.0.0 1.2 4.0.0 0.7 2.0 1.0 0.0 0 10 20 0 40 0.0 0.2 0 10 20 0 40 Figure 4. Overlay of and chromatograms for different products. 6

Conclusions HSGC-MS method was developed for qualitative of consumer products. Comparative data was generated using static and dynamic headspace techniques for consumer products. Both technique can be used as valuable tools for analyzing a variety of matrices. Statistical evaluation of the data showed that the dynamic HS technique method was more superior with respect to sensitivity and reliability as compared to static HS technique. The unique configuration of flow lines and the HS oven enable the analysis of high boiling point compounds while minimizing carryover. In addition, by using a trap function that incorporates an electronic cooling mechanism, it is possible to concentrate the headspace gas, which enables high-sensitivity analysis of low to high boiling point compounds. Disclaimer: The products and applications in this presentation are intended for Research Use Only (RUO). Not for use in diagnostic procedures. First Edition: December, 2017 Shimadzu Corporation, 2017