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*Corresponding Author: Wenhong Zhao, College of Light Industry and Food Sciences, Zhongkai University of Agriculture and Engineering, Guangzhou, 510225, China.
Citation: Hao Jiang, Mutang Zhang, Junjie Ye, Xinman Zhan, Heming Qi., et all (2023), Optimization of Volatile component Analysis Technique for Salt-Baked Chicken, J. Nutrition and Food Processing, 6(2); DOI:10.31579/2637-8914/133
Copyright: © 2023 Wenhong Zhao, This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Received: 21 March 2023 | Accepted: 10 April 2023 | Published: 18 April 2023
Keywords: salt-baked chicken; volatile component; headspace solid-phase microextraction; optimization
A Method for volatile components analysis of salt-baked chicken was established by using the headspace solid-phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS) technology. The optimum process is determined by analysis of single factor. Specifically, the SPME fiber (carboxen/polydimethylsiloxane, CAR/PDMS, 75 µm) was used in the extraction of the volatile compounds in salt-baked chicken. Meantime, equilibrium time and extraction temperature were 10 min and 60 °C, respectively. For the rest, the extractions were carried out for 30 min and desorption of the samples for 5 min. After preliminary analysis, 65 volatile components were detected in the salt-baked chicken. The extraction parameters were reasonable, feasible and practical, which was conducive to further qualitative and quantitative analysis of aroma substances in salt-baked chicken.
Salt-baked chicken is a Hakka dish with Cantonese characteristics in China. It is quite palatable and tender meat with high fat content [1]. As for the recipe of salt-baked chicken, kosher salt was used as the heat transfer medium to bake the chicken which had marinated with seasoning [2, 3]. Nowadays, the sales volume of salt-baked chicken was among the top of deli meat, which was made widely in our country. High baking temperatures and long cooking time would lead to a great thermal degradation/oxidation of lipids in salt-baked chicken, generating high content of lipid-derived volatile substances [4]. The flavour of the salt-baked chicken was an important indicator of its sensory quality. Therefore, it was of great significance to clarify the volatile components of salt-baked chicken, in order to further explore its flavor formation mechanism and improve its preparation technology. However, there were little research on the volatile components and flavour of salt-baked chicken at home and abroad.
Nowadays, solid-phase microextraction (SPME) has been widely used in odor research of deli meat products. SPME had the advantages of high efficiency, green and simple operation. A series of technological processes such as extraction, enrichment and injection could be completed on the SPME device alone, which greatly reduced the analysis time. Meantime, compared with static headspace, it enriched volatile organic compounds at a lower concentration [5, 6]. Zhang et al. used electronic nose, electronic tongue and the headspace solid-phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS) technology to evaluate the volatile flavor components of sugar-smoked chicken drumsticks, and 75 volatile compounds were identified [7]. The volatile compounds in braised pork with brown sauce were also revealed by HS-SPME-GC-MS, and 109 volatile flavour compounds were detected [8]. These data intuitively demonstrated the variation of the type and concentration of the volatile compounds that affect the flavour of meat products, which had an important effect on the exploration of flavour components.
The volatile flavor components of salt-baked chicken were complex and needed to be analyzed by precise instruments such as gas chromatography and mass spectrometry. Therefore, the detection method of SPME extraction technology combined with precise instruments has been recognized by researchers [9]. Consequently, the HS-SPME-GC-MS technique was manipulated to establish an analytical method for volatile components of salt-baked chicken in this research. The optimum sampling conditions were investigated, including the variety of SPME fiber, the extracting temperature, the equilibrium time, the extraction time and the desorption time. Subsequently, the volatile flavor components of salt-baked chicken were preliminarily analyzed by the optimized process. This research explored the optimum technology of qualitative and quantitative analysis of aroma substances in salt-baked chicken, so as to provide experimental and theoretical basis for improving the flavour and promoting industrial production of salt-baked chicken.
2.1 Ethics statement
The housing and treatment of the animals were carried out following national and international laws as well as with institutional guidelines. Since all chicken used in this study were obtained from a restaurant (Meizhou, Guangdong). We were explicitly issued a formal waiver of ethics approval.
2.2 Materials and reagents
Salt-baked chicken (white feather broilers) were purchased from a restaurant in Meizhou, Guangdong. 2-Methyl-3-heptanone (AR) was purchased from Dr. Ehrenstorfer Gmbh (Augsburg, Germany). A standard mixture solution containing C7-C40 hydrocarbons (1000 mg/L, dissolved in n-Alkane) was purchased from o2si smart solutions (Charleston, SC, USA).
2.3 Instruments and equipment
The extraction of the volatile compounds was performed using SPME with a manual microinjection needle (5190-1483, Guosheng Experimental Instrument Factory, China) and was separated, identified and quantified in a gas chromatograph (7890A GC-System, Agilent Technologies, Santa Clara, CA, USA) equipping with a mass selective detector (5975C MSD, Agilent Technologies). The magnetic stirrer (85-2A) was supplied by Guosheng Experimental Instrument Factory.
2.4 SPME Extraction
SPME fiber, extraction temperature, equilibrium time, extraction time and desorption time had the potential to affect the volatile aroma components. Meantime, the optimal detection conditions of the volatile aroma components of salt-baked chicken were explored by HS-SPME-GC-MS [10]. Briefly, the sample (4.0 g) was added to a 20 mL headspace vial (CNW Technologies, Duesseldorf, Germany). Next 2-methyl-3-heptanone (1 µL; 0.812 µg/µL in ethanol) was added as the internal standard (IS). The mixture solution was homogenized in a magnetic thermostatic water bath and the volatile compounds were detected by GC-MS.
2.5 Statistical analysis
Data are presented as the least-squared means of the three replicates with the standard error of the mean (SE).Statistical analysis was performed using Tukey–Kramer multiple-comparison tests as indicated in the table and figure legend. The JMP13 software was used to analyze the statistical significance level (p < 0>
Figure 1: The effect of using different SPME conditions ((A) SPME fiber, (B) extracting temperature, (C) equilibrium time, (D)extraction time and (E) desorption time) on extraction efficiency. The total peak area and the effective number of peaks obtained by GC-MS were compared and analyzed. Values were shown as the mean ± SE (n = 3). Different letters within the histogram of the same color indicates significantly differences by Tukey-Kramer multiple comparison test (p < 0>
3.1 The optimum conditions of SPME fibers
The SPME fiber is the core of the SPME extraction device. Different extraction coating materials have different adsorption capacities. The effects of 5 kinds of SPME fiber (50/30 µm thickness of divinylbenzene (DVB)/ carboxen (CAR)/ polydimethylsiloxane (PDMS), 65 µm thickness of PDMS/ DVB, 75 µm thickness of CAR/ PDMS, 85 µm thickness of polyacrylate (PA) or 100 µm thickness of CAR/ PDMS) on chicken flavour compounds were explored. For the rest, the extractions were carried out for 10 min, after equilibration of the samples for 30 min, and desorption of the samples for 5 min at 40°C. As shown in Figure. 1(A), the fiber (CAR/PDMS, 75 µm thickness) showed greater adsorption capacity, which had the largest total peak area and more effective number of peaks. PDMS/ DVB (65 µm thickness) had the very small total peak area compared to the maximum value although it had the largest number of effective peaks. So, according to the total amount of volatile compounds, the fiber of 75 µm thickness of CAR/ PDMS was chosen in follow-up extraction experiments.
RT (min) | Compound Name | CAS | Matching degree (%) | content（μg/g） | Threshold Value (mg/kg) | |
| 1 | 7.08 | Hexanal | 66-25-1 | 91 | 0.296322893 | 0.21 |
| 2 | 9.08 | Meta-xylene | 108-38-3 | 95 | 0.012761039 | 5.5 |
| 3 | 9.16 | Ortho-xylene | 95-47-6 | 89 | 0.005919554 | 3 |
| 4 | 9.86 | 2-Methyl-3-heptanone | 13019-20-0 | 91 | 0.20298 | - |
| 5 | 10.49 | Heptaldehyde | 111-71-7 | 80 | 0.013436485 | 0.005 |
| 6 | 11.27 | Cinene | 005989-27-5 | 94 | 0.071761278 | 0.5 |
| 7 | 12.6 | 2-Pentylfuran | 3777-69-3 | 93 | 0.043429049 | 0.0048 |
| 8 | 12.95 | Styrene | 100-42-5 | 97 | 0.022595713 | 0.022 |
| 9 | 13.57 | 2-Methylpyrazine | 109-08-0 | 90 | 0.011440678 | 0.25 |
| 10 | 14.18 | 2-Octanone | 111-13-7 | 94 | 0.004273606 | 0.05 |
| 11 | 14.25 | Octyl aldehyde | 124-13-0 | 91 | 0.094986742 | 0.0001 |
| 12 | 15.44 | trans-2-Heptenal | 57266-86-1 | 93 | 0.00421757 | 0.15 |
| 13 | 15.64 | 2, 3-Dimethylpyrazine | 5910-89-4 | 86 | 0.00317469 | 0.1 |
| 14 | 15.84 | 2,3-Octanedione | 585-25-1 | 80 | 0.174331578 | - |
| 15 | 16.81 | Hexanol | 111-27-3 | 90 | 0.066548497 | 0.2 |
| 16 | 17.53 | 3-Ethylpyridine | 536-78-7 | 95 | 0.003454931 | - |
| 17 | 18.03 | Nonyl aldehyde | 124-19-6 | 94 | 0.121707269 | 0.0035 |
| 18 | 18.34 | 2, 3, 5-Trimethylpyrazine | 14667-55-1 | 90 | 0.008431219 | 0.01 |
| 19 | 18.432 | Tetradecyl | 629-59-4 | 91 | 0.013979536 | 300 |
| 20 | 18.6 | (Z)-3-Ethyl-2-methyl-1, 3-hexadiene | 61142-36-7 | 94 | 0.026453806 | - |
| 21 | 19.11 | 2-Octene aldehyde | 20664-46-4 | 84 | 0.032362144 | 0.05 |
| 22 | 19.74 | 3-Ethyl-2, 5-dimethylpyrazine | 13360-65-1 | 93 | 0.007560117 | 0.025 |
| 23 | 19.88 | Acetic acid | 64-19-7 | 64 | 0.0041039 | 900 |
| 24 | 20.17 | Furfural | 98-01-1 | 87 | 0.164034001 | 0.01 |
| 25 | 20.36 | Heptanol | 111-70-6 | 80 | 0.034629878 | 0.2 |
| 26 | 21.7 | Coumarone | 271-89-6 | 93 | 0.038124762 | - |
| 27 | 21.84 | Decanal | 112-31-2 | 87 | 0.01612584 | 0.005 |
| 28 | 22.1 | Pentadecane | 629-62-9 | 96 | 0.004148139 | - |
| 29 | 22.41 | Benzaldehyde | 100-52-7 | 96 | 0.094545994 | 0.3 |
| 30 | 23.43 | trans-2-Nonenal | 18829-56-6 | 95 | 0.009296848 | 0.000065 |
| 31 | 23.59 | 3-Butyl-cyclopentanone | 57283-81-5 | 96 | 0.009776674 | - |
| 32 | 24.64 | 2-Methyl-2,3-dihydro-1-benzofuran | 1746-11-8 | 91 | 0.00119869 | - |
| 33 | 24.73 | α-Cedrene | 469-61-4 | 98 | 0.001751652 | - |
| 34 | 25.11 | Octanol | 111-87-5 | 87 | 0.067109201 | 0.054 |
| 35 | 25.58 | 2-Butylpyridine | 5058-19-5 | 87 | 0.005290704 | - |
| 36 | 25.96 | 2-Methylbenzofuran | 4265-25-2 | 94 | 0.009149949 | - |
| 37 | 27.43 | 2-Acetylpyrazine | 22047-25-2 | 96 | 0.01017287 | 0.1 |
| 38 | 28.33 | Acetophenone | 98-86-2 | 93 | 0.037623924 | 3 |
| 39 | 29.59 | Nonyl alcohol | 143-08-8 | 91 | 0.012277373 | 0.002 |
| 40 | 29.73 | O-Methylacetophenone | 577-16-2 | 94 | 0.004693842 | - |
| 41 | 31.62 | β-Bisabolene | 000495-61-4 | 84 | 0.009819877 | 0.05 |
| 42 | 33.18 | α-curcumene | 644-30-4 | 98 | 0.003313802 | - |
| 43 | 33.57 | Methoxy-phenyl-oxime | 91 | 0.016621356 | - | |
| 44 | 34.31 | (E,E)-2,4-Decadienal | 25152-84-5 | 95 | 0.008580047 | 0.00003 |
| 45 | 34.78 | Anethole | 104-46-1 | 98 | 0.037386118 | 0.1 |
| 46 | 35.62 | Caproic acid | 142-62-1 | 90 | 0.008312433 | 80 |
| 47 | 35.7 | Guaiacol | 90-05-1 | 97 | 0.010156153 | - |
| 48 | 36.19 | Benzyl alcohol | 100-51-6 | 97 | 0.001609666 | 5.5 |
| 49 | 37.25 | γ-Symplectic lactone | 104-50-7 | 90 | 0.003109064 | 0.095 |
| 50 | 37.91 | 3-(4-Methylphenyl) -2-propenal | 1504-75-2 | 87 | 0.001750304 | - |
| 51 | 38.46 | P-Methyl guaiacol | 93-51-6 | 95 | 0.001777907 | 0.01 |
| 52 | 38.71 | Heptanoic acid | 111-14-8 | 81 | 0.001117007 | 0.1 |
| 53 | 38.86 | 2-Acetylpyrrole | 1072-83-9 | 83 | 0.00084633 | 100 |
| 54 | 39.15 | Diphenyl | 92-52-4 | 91 | 0.001400275 | - |
| 55 | 39.81 | Phenol | 108-95-2 | 93 | 0.011791037 | 5.5 |
| 56 | 40.1 | anisaldehyde | 123-11-5 | 96 | 0.012729052 | 0.01 |
| 57 | 40.34 | γ-Nonyl lactone | 104-61-0 | 93 | 0.001260664 | 0.065 |
| 58 | 41.77 | m-Cresol | 106-44-5 | 95 | 0.001289311 | 0.002 |
| 59 | 42.69 | Cedrol | 77-53-2 | 98 | 0.001623855 | - |
| 60 | 43.04 | Ethyl cinnamate | 4192-77-2 | 98 | 0.000381516 | 0.00006 |
| 61 | 44.05 | 2-Ethylphenol | 90-00-6 | 90 | 0.000574448 | 0.03 |
| 62 | 44.23 | Pelargonic acid | 112-05-0 | 93 | 0.001463142 | 1.5 |
| 63 | 45.04 | Cadalene | 483-78-3 | 95 | 0.000750931 | - |
| 64 | 45.93 | ar-Turmerone | 532-65-0 | 95 | 0.000690779 | - |
| 65 | 47.08 | 4-Methyl-5-beta-hydroxyethyl thiazole | 137-00-8 | 97 | 0.014946091 | 10.8 |
RT: Retention Time; Matching value meant the matching degree of the compound to its chromatographic peak and mass spectrum peak; Threshold value meant the lowest concentration of the flavour substance which would be felt by human body.
Table 1: Qualitative and quantitative analysis of volatile compounds in salt-baked chicken
3.2 The optimum conditions of the extracting temperature
Extraction temperature is a significant factor in affecting extraction speed and efficiency. The effects of different extraction temperatures on the detection of volatile flavour compounds in salt-baked chicken were evaluated. Samples were extracted at different extraction temperatures (50℃, 55℃, 60℃, 65℃, 70℃) under the conditions of SPME fiber with 75 µm, CAR/PDMS, fixing equilibrium time at 10 min, extraction time at 30 min and desorption time at 5 min.
When the extraction temperature was between 50-60℃, the number of detected effective peaks showed an increasing trend with a rise in temperature and reached the maximum value at 60℃ (Fig. 1(B)).At the extraction temperature of 60℃, it had the biggest effective peaks. Meantime, the total peak area increased gradually with the increasing temperature, and became almost stable after 55℃. Interestingly, as the temperature further increased, the number of effective peaks decreased and reached a lower value at 65℃. Thus, 60℃ was the optimal extraction temperature.
3.3 The optimum conditions of the SPME equilibrium time
Equilibration time was affected by interactions between the solid, liquid and gas phases in the sample. This step would explore the effect of different equilibration time on the detection of volatile flavour compounds in salt-baked chicken. Samples were extracted with different equilibrium times (5 min, 10 min, 15 min, 20 min, 25 min) fixing extraction time and desorption time at 30 min and 5 min, respectively. When the equilibration time was 10 min, the number of effective peaks reached the maximum (Fig. 1(C)). After 10 min, the number of effective peaks gradually decreased. So, the equilibrium time of 10 min was chosen in follow-up extraction experiments.
3.4 The optimum conditions of the SPME extraction time
The extraction time of SPME fiber is a key factor affecting the extraction results as well. The extraction was repeated by varying the extraction times (20 min, 25 min, 30 min, 35 min, 40 min). The desorption time was set at 5 min. As the figure 1(D) showed, the total peak area increased significantly with the prolonging of time until 35 minutes. After that, the total peak area tended to decrease. In addition, the number of effective peaks increased with the extraction time extension, and the peak value was obtained at 30 minutes. Generally, 30 min is the optimal extraction time with the largest number of effective peaks.
3.5 The optimum conditions of the SPME desorption time
This step explored the effect of different desorption times of the SPME fiber in the GC injection port on the detection results. Using the parameters determined above (SPME fiber, extracting temperature, equilibrium time and extraction time), chicken samples were extracted at different desorption times from 1 to 9 min (1 min, 3 min, 5min, 7min, 9 min). With the prolongation of the desorption time, the number of effective peaks represented as a bell-shaped curve, and reached the maximum value at 3-5 minutes (Fig. 1(E)). Furthermore, the total peak area was significantly high when the desorption time was 5 min. So, the desorption time was selected as 5 min.
3.6 Analysis of volatile components in salt-baked chicken
According to the optimized HS-SPME extraction conditions, the volatile components in the salt-baked chicken samples were extracted and desorbed. The volatile components in the salt-baked chicken samples were separated and identified by GC-MS. The qualitative and quantitative analysis of volatile compounds were performed by comparing MS with the NIST08 library (National Institute of Standards and Technology, Gaithersburg) and by comparing the chromatographic peak area of volatile substances with the internal standard [11]. Detailed quantitative principles of GC-MS referred to the article of Jiang et al [12]. According to the optimized SPME extraction conditions, 65 volatile flavour compounds were found in salt-baked chicken (table1). These volatile flavour compounds included aldehydes (12), alcohols (7), alkanes (12), heterocycles (15), ketones (7), acids (4), phenols (5) and esters (3).
In the optimizing of the SPME fibers, the phenomenon which PDMS/ DVB (65 µm thickness) had the very small total peak area and the largest number of effective peaks was also reported by Yu et al [13]. In the volatile flavour detection experiment of traditional smoke-cured bacon, it was also found that CAR/PDMS (75 µm thickness) coated fiber extracted the higher total peak area of volatile compounds than 65 µm thickness of PDMS/ DVB and the PDMS/ DVB (65 µm thickness) was given up because of its total peak area [13].
Next, a possible explanation for the phenomenon of the lower value at extracting temperature of 65℃ was that high temperature would accelerate solvent containing flavour substances evaporation and some flavour substances were decomposed [14]. Meantime, high temperature promoted the enrichment and adsorption of target compounds by SPME fiber. However, extraction is an exothermic process. As the temperature increased, the distribution coefficient of volatile substances between the SPME fiber and the sample would decrease, resulting in a reduced number of effective peaks. At the same time, the adsorptive capacity of the analyte and the sensitivity were reduced. This result was similar to the conclusion of Liang et, al [15]. The extraction efficiency showed an obvious increase from 40-80℃. However, when the extraction temperature was further increased to 100℃, no significant increase was observed [15]. Another possible explanation was that some volatile compounds were denatured and cracked at high temperatures, affecting the accuracy of the number of effective peaks [16].
Furthermore, the changes of volatile species in the chicken took time to reach equilibrium during the process of headspace absorption. Equilibration time was affected by the time for the sample to reach equilibrium in three-phase (the solid, liquid and gas phases) during the process of headspace absorption. The extraction efficiency increased with increasing equilibration time. However, the target sample would redissolve in the solvent if took a long time to equilibrate, resulting in lower extraction efficiency [16]. Interestingly, under the equilibration time of 20 min, the total peak area reached a maximum value. The phenomenon probably because some volatile compounds were redissolved with further increase in the equilibration time. This possible explanation needs to be confirmed in the future.
Moreover, the number of effective peaks and the total peak area increased with the extraction time extension before reaching the extraction equilibrium state. Therefore, during the extraction time of 35 minutes, some compounds might be redissolved, while some analytes continued to be adsorbed, so that the total concentration still increased. Li, T et al measured the effect of different extraction times of SPME on the extraction of volatile organic compounds (toluene, ethylbenzene and o-xylene) and found that the peak area of each analyte increased significantly within the extraction time of 5-15 min. However, excessive extraction times no longer increased extraction efficiency and sometimes caused desorption after 15 min [17, 18]. Similarly, at this moment, the degree of separation had shown a downward trend, and influenced the quantification of the peak area method.
What’s more, in the matter of the SPME desorption time, the volatile substances evaporated at 3-5 minutes, but the concentrations gradually grew, which they could not be absorbed in a short time [19]. Meantime, too long absorption time would affect the service life of the SPME fiber [20]. Therefore, a lack of desorption time could easily lead to incomplete desorption, affecting the peak area. Some volatile aroma components would be decomposed with the passage of time. Thereby, the service life of the SPME fiber and the separation effect were affected.
Among the flavoring substances, hexanal, 2-methyl -3-heptanone, 2, 3-octanedione, furfural, nonyl aldehyde, octyl aldehyde and benzaldehyde were the main volatile components with high content. Meantime, the volatile flavour compounds (65) which detected by the optimum process condition were obviously more than the volatile flavour compounds (36) of salt baked chickens in research of Wu et al [21]. The results of this study provided credible data basis for the accurate evaluation of aroma components of salt-baked chicken, and provided reference for formation improvement and industrial production of salt-baked chicken.
In this research, the extraction conditions of SPME for volatile components analysis of salt-baked chicken were optimized. After thorough consideration, the volatile compounds of salt-baked chicken were extracted by SPME fiber of 75 µm, CAR/PDMS, equilibrium time and extraction temperature were 10 min and 60 °C. Furthermore, extraction time and desorption time were 30 min and 5 min, respectively. Then the HS-SPME-GC-MS method was established and further volatile components in salt-baked chicken were detected. The result reflected 65 volatile flavour compounds were identified (12 aldehydes, 7 alcohols, 12 alkanes, 15 heterocycles, 7 ketones, 4 acids, 5 phenols and 3 esters). Based on the analysis of salt-baked chicken by HS-SPME-GC-MS, the material data affecting the flavour were obtained, which provided a theoretical reference for the preparation and industrial production of salt-baked chicken products.
Wenhong Zhao, Weidong Bai, Xiaofang Zeng, Heming Qi and Min Qian conceived and designed the experiments; Junjie Ye and Xinman Zhan performed the experiments; Mutang Zhang, Hao Jiang, Junjie Ye analyzed the data and wrote the manuscript. This work was supported by the pigeon industry key technology research and demonstration Integration, Grant Number 2020B0202080002 (Xiaofang Zeng) from Guangdong Province key field research and development program project, Guangdong Provincial Key Laboratory of Lingnan Specialty Food Science and Technology, Grant Number 2021B1212040013, China, Key Realm R&D Program of GuangDong Province, Grant Number 2020B0202080002, China and Key Research Base of Sichuan Province -- Sichuan Food Development Research Center, Grant Number CC22Z18, China.
The data that support the findings of this study are available from the corresponding author upon reasonable request.
None of the authors has any financial or other interest that could inappropriately influence or bias the content of this manuscript.
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"We recently published an article entitled “Influence of beta-Cyclodextrins upon the Degradation of Carbofuran Derivatives under Alkaline Conditions" in the Journal of “Pesticides and Biofertilizers” to show that the cyclodextrins protect the carbamates increasing their half-life time in the presence of basic conditions This will be very helpful to understand carbofuran behaviour in the analytical, agro-environmental and food areas. We greatly appreciated the interaction with the editor and the editorial team; we were particularly well accompanied during the course of the revision process, since all various steps towards publication were short and without delay".
I would like to express my gratitude towards you process of article review and submission. I found this to be very fair and expedient. Your follow up has been excellent. I have many publications in national and international journal and your process has been one of the best so far. Keep up the great work.
We are grateful for this opportunity to provide a glowing recommendation to the Journal of Psychiatry and Psychotherapy. We found that the editorial team were very supportive, helpful, kept us abreast of timelines and over all very professional in nature. The peer review process was rigorous, efficient and constructive that really enhanced our article submission. The experience with this journal remains one of our best ever and we look forward to providing future submissions in the near future.
I am very pleased to serve as EBM of the journal, I hope many years of my experience in stem cells can help the journal from one way or another. As we know, stem cells hold great potential for regenerative medicine, which are mostly used to promote the repair response of diseased, dysfunctional or injured tissue using stem cells or their derivatives. I think Stem Cell Research and Therapeutics International is a great platform to publish and share the understanding towards the biology and translational or clinical application of stem cells.
I would like to give my testimony in the support I have got by the peer review process and to support the editorial office where they were of asset to support young author like me to be encouraged to publish their work in your respected journal and globalize and share knowledge across the globe. I really give my great gratitude to your journal and the peer review including the editorial office.
I am delighted to publish our manuscript entitled "A Perspective on Cocaine Induced Stroke - Its Mechanisms and Management" in the Journal of Neuroscience and Neurological Surgery. The peer review process, support from the editorial office, and quality of the journal are excellent. The manuscripts published are of high quality and of excellent scientific value. I recommend this journal very much to colleagues.
Dr.Tania Muñoz, My experience as researcher and author of a review article in The Journal Clinical Cardiology and Interventions has been very enriching and stimulating. The editorial team is excellent, performs its work with absolute responsibility and delivery. They are proactive, dynamic and receptive to all proposals. Supporting at all times the vast universe of authors who choose them as an option for publication. The team of review specialists, members of the editorial board, are brilliant professionals, with remarkable performance in medical research and scientific methodology. Together they form a frontline team that consolidates the JCCI as a magnificent option for the publication and review of high-level medical articles and broad collective interest. I am honored to be able to share my review article and open to receive all your comments.
“The peer review process of JPMHC is quick and effective. Authors are benefited by good and professional reviewers with huge experience in the field of psychology and mental health. The support from the editorial office is very professional. People to contact to are friendly and happy to help and assist any query authors might have. Quality of the Journal is scientific and publishes ground-breaking research on mental health that is useful for other professionals in the field”.
Dear editorial department: On behalf of our team, I hereby certify the reliability and superiority of the International Journal of Clinical Case Reports and Reviews in the peer review process, editorial support, and journal quality. Firstly, the peer review process of the International Journal of Clinical Case Reports and Reviews is rigorous, fair, transparent, fast, and of high quality. The editorial department invites experts from relevant fields as anonymous reviewers to review all submitted manuscripts. These experts have rich academic backgrounds and experience, and can accurately evaluate the academic quality, originality, and suitability of manuscripts. The editorial department is committed to ensuring the rigor of the peer review process, while also making every effort to ensure a fast review cycle to meet the needs of authors and the academic community. Secondly, the editorial team of the International Journal of Clinical Case Reports and Reviews is composed of a group of senior scholars and professionals with rich experience and professional knowledge in related fields. The editorial department is committed to assisting authors in improving their manuscripts, ensuring their academic accuracy, clarity, and completeness. Editors actively collaborate with authors, providing useful suggestions and feedback to promote the improvement and development of the manuscript. We believe that the support of the editorial department is one of the key factors in ensuring the quality of the journal. Finally, the International Journal of Clinical Case Reports and Reviews is renowned for its high- quality articles and strict academic standards. The editorial department is committed to publishing innovative and academically valuable research results to promote the development and progress of related fields. The International Journal of Clinical Case Reports and Reviews is reasonably priced and ensures excellent service and quality ratio, allowing authors to obtain high-level academic publishing opportunities in an affordable manner. I hereby solemnly declare that the International Journal of Clinical Case Reports and Reviews has a high level of credibility and superiority in terms of peer review process, editorial support, reasonable fees, and journal quality. Sincerely, Rui Tao.
Clinical Cardiology and Cardiovascular Interventions I testity the covering of the peer review process, support from the editorial office, and quality of the journal.
Clinical Cardiology and Cardiovascular Interventions, we deeply appreciate the interest shown in our work and its publication. It has been a true pleasure to collaborate with you. The peer review process, as well as the support provided by the editorial office, have been exceptional, and the quality of the journal is very high, which was a determining factor in our decision to publish with you.
The peer reviewers process is quick and effective, the supports from editorial office is excellent, the quality of journal is high. I would like to collabroate with Internatioanl journal of Clinical Case Reports and Reviews journal clinically in the future time.
Clinical Cardiology and Cardiovascular Interventions, I would like to express my sincerest gratitude for the trust placed in our team for the publication in your journal. It has been a true pleasure to collaborate with you on this project. I am pleased to inform you that both the peer review process and the attention from the editorial coordination have been excellent. Your team has worked with dedication and professionalism to ensure that your publication meets the highest standards of quality. We are confident that this collaboration will result in mutual success, and we are eager to see the fruits of this shared effort.
Dear Dr. Jessica Magne, Editorial Coordinator 0f Clinical Cardiology and Cardiovascular Interventions, I hope this message finds you well. I want to express my utmost gratitude for your excellent work and for the dedication and speed in the publication process of my article titled "Navigating Innovation: Qualitative Insights on Using Technology for Health Education in Acute Coronary Syndrome Patients." I am very satisfied with the peer review process, the support from the editorial office, and the quality of the journal. I hope we can maintain our scientific relationship in the long term.
Dear Monica Gissare, - Editorial Coordinator of Nutrition and Food Processing. ¨My testimony with you is truly professional, with a positive response regarding the follow-up of the article and its review, you took into account my qualities and the importance of the topic¨.
Dear Dr. Jessica Magne, Editorial Coordinator 0f Clinical Cardiology and Cardiovascular Interventions, The review process for the article “The Handling of Anti-aggregants and Anticoagulants in the Oncologic Heart Patient Submitted to Surgery” was extremely rigorous and detailed. From the initial submission to the final acceptance, the editorial team at the “Journal of Clinical Cardiology and Cardiovascular Interventions” demonstrated a high level of professionalism and dedication. The reviewers provided constructive and detailed feedback, which was essential for improving the quality of our work. Communication was always clear and efficient, ensuring that all our questions were promptly addressed. The quality of the “Journal of Clinical Cardiology and Cardiovascular Interventions” is undeniable. It is a peer-reviewed, open-access publication dedicated exclusively to disseminating high-quality research in the field of clinical cardiology and cardiovascular interventions. The journal's impact factor is currently under evaluation, and it is indexed in reputable databases, which further reinforces its credibility and relevance in the scientific field. I highly recommend this journal to researchers looking for a reputable platform to publish their studies.
Dear Editorial Coordinator of the Journal of Nutrition and Food Processing! "I would like to thank the Journal of Nutrition and Food Processing for including and publishing my article. The peer review process was very quick, movement and precise. The Editorial Board has done an extremely conscientious job with much help, valuable comments and advices. I find the journal very valuable from a professional point of view, thank you very much for allowing me to be part of it and I would like to participate in the future!”
Dealing with The Journal of Neurology and Neurological Surgery was very smooth and comprehensive. The office staff took time to address my needs and the response from editors and the office was prompt and fair. I certainly hope to publish with this journal again.Their professionalism is apparent and more than satisfactory. Susan Weiner
My Testimonial Covering as fellowing: Lin-Show Chin. The peer reviewers process is quick and effective, the supports from editorial office is excellent, the quality of journal is high. I would like to collabroate with Internatioanl journal of Clinical Case Reports and Reviews.
My experience publishing in Psychology and Mental Health Care was exceptional. The peer review process was rigorous and constructive, with reviewers providing valuable insights that helped enhance the quality of our work. The editorial team was highly supportive and responsive, making the submission process smooth and efficient. The journal's commitment to high standards and academic rigor makes it a respected platform for quality research. I am grateful for the opportunity to publish in such a reputable journal.
My experience publishing in International Journal of Clinical Case Reports and Reviews was exceptional. I Come forth to Provide a Testimonial Covering the Peer Review Process and the editorial office for the Professional and Impartial Evaluation of the Manuscript.
