7 research outputs found
การพัฒนาศักยภาพเมล็ดทุเรียนในผลิตผลิตภณัฑ์ขนมไทย
Get PDFรายงานวิจัย -- มหาวิทยาลัยเทคโนโลยีราชมงคลพระนคร, 2559Research Title : Developing the potential of durian peel in bakery products Author : Chakkrawut Bhoosem Photchanee Bunna Apinya Manarote and Prassanee Tubbiyam Department : Food and Nutrition Faculty : Home Economics Technology Academic year :
The objective of this research to study the process of durian seed including of Durian seed in syrup, Look Choup Durian Seed, Chinese Mochi Cake Durian seed filling, Durian Seed Custard and Meung Durian Seed. To determine the quality of processed food products from Durian seed. To study consumer acceptance (Consumer test) on food products from durian seed. Processed food products from durian seed used in the trial, including of Durian seed in syrup, Look Choup Durian Seed, Chinese Mochi Cake Durian seed filling, Durian Seed Custard and Meung Durian Seed. The substitution of main ingredients with durian seed products, the sample substitute at percent to percent panelists recognized that the percent to percent except sample to recognize. However, the replacement of percent on the amount of compensation increases. Make an example of a more solid texture. The panelists acknowledged the least clear. And not according to the way that it should be. However, durian seed supplementation resulted in increased amount of protein, which is beneficial to the health of consumers.
Acceptance testing of consumer substitution of wheat flour with durian peel powder products in bakeries, by means of random chance that the test of more than percent of the product acceptance bakeries are replacement of wheat flour with durian rind powder.
For bakery products, technology transfer from Japan selected durian powder at the Faculty of Economics of Technology. Trainee There is satisfaction in all aspects of technology transfer. Keywords: durian seed, Thai dessertRajamangala University of Technology Phra Nakho
Stability Analysis of Multiple LEDs Dimming Circuits: An Interaction between an LC Input Filter and Two Buck Converters
No full textAbstractThis paper proposes an average modeling of LED dimming circuits controlled by an indirect sliding mode technique. The circuit and control parameters that affect a multiple LED dimming system's stability are studied. The dimming system comprises two output-capacitorless buck converters and each converter connected to two strings of LEDs as a load. These dimming buck converters are connected to a 48V power source via an LC filter to reduce the input ripple current. It is known that fast response dc-dc converter might lead to unstable operation of the system due to its negative input resistance characteristic. This paper investigates the control parameters of the sliding control that affect dynamics of a DC bus due to the change of the operating point of LED. The theoretical model is validated through experimental results obtained from the test bench
Development and assessment of a Real-Time PCR assay for the rapid and sensitive detection of a novel thermotolerant bacterium, Lactobacillus thermotolerans, in chicken feces
Get PDFA new real-time PCR assay was successfully developed using a TaqMan fluorescence probe for specific detection and enumeration of a novel bacterium, Lactobacillus thermotolerans, in chicken feces. The specific primers and probe were designed based on the L. thermotolerans 16S rRNA gene sequences, and these sequences were compared to those of all available 16S rRNA genes in the GenBank database. The assay, targeting 16S rRNA gene, was evaluated using DNA from a pure culture of L. thermotolerans, DNA from the closely related bacteria Lactobacillus mucosae DSM 13345T and Lactobacillus fermentum JCM 1173T, and DNA from other lactic acid bacteria in quantitative experiments. Serial dilutions of L. thermotolerans DNA were used as external standards for calibration. The minimum detection limit of this technique was 1.84 x 103 cells/ml of an L. thermotolerans pure culture. The assay was then applied to chicken feces in two different trials. In the first trial, the cell population was 104 cells/g feces on day 4 and 105 cells/g feces on days 11 to 18. However, cell populations of 106 to 107 cells/g feces were detected in the second trial. The total bacterial count, measured by 4',6-diamidino-2-phenylindole (DAPI) staining, was approximately 1011 cells/g feces. These results suggest that in general, L. thermotolerans is a normal member of the chicken gut microbiota, although it is present at relatively low levels in the feces
Publisher Correction: Myzorhynchus series of Anopheles mosquitoes as potential vectors of Plasmodium bubalis in Thailand (Scientific Reports, (2022), 12, 1, (5747), 10.1038/s41598-022-09686-9)
No full textThe original version of this Article contained errors in the order of the Figures. Figures 2 and 3 were published as Figures 3 and 2. As a result, the Figure legends were incorrect. The original Figures 2 and 3 and accompanying legends appear below. The original Article has been corrected. © 2022, The Author(s)
Myzorhynchus series of Anopheles mosquitoes as potential vectors of Plasmodium bubalis in Thailand
No full textUngulate malaria parasites and their vectors are among the least studied when compared to other medically important species. As a result, a thorough understanding of ungulate malaria parasites, hosts, and mosquito vectors has been lacking, necessitating additional research efforts. This study aimed to identify the vector(s) of Plasmodium bubalis. A total of 187 female mosquitoes (133 Anopheles spp., 24 Culex spp., 24 Aedes spp., and 6 Mansonia spp. collected from a buffalo farm in Thailand where concurrently collected water buffalo samples were examined and we found only Anopheles spp. samples were P. bubalis positive. Molecular identification of anopheline mosquito species was conducted by sequencing of the PCR products targeting cytochrome c oxidase subunit 1 (cox1), cytochrome c oxidase subunit 2 (cox2), and internal transcribed spacer 2 (ITS2) markers. We observed 5 distinct groups of anopheline mosquitoes: Barbirostris, Hyrcanus, Ludlowae, Funestus, and Jamesii groups. The Barbirostris group (Anopheles wejchoochotei or Anopheles campestris) and the Hyrcanus group (Anopheles peditaeniatus) were positive for P. bubalis. Thus, for the first time, our study implicated these anopheline mosquito species as probable vectors of P. bubalis in Thailand. © 2022, The Author(s)
Tissue Microbiome Profiling Identifies an Enrichment of Specific Enteric Bacteria in Opisthorchis viverrini Associated Cholangiocarcinoma
No full textAbstractCholangiocarcinoma (CCA) is the primary cancer of the bile duct system. The role of bile duct tissue microbiomes in CCA tumorigenesis is unestablished. To address this, sixty primary CCA tumors and matched normals, from both liver fluke (Opisthorchis viverrini) associated (OVa, n=28) and non-O. viverrini associated (non-OVa, n=32) cancers, were profiled using high-throughput 16S rRNA sequencing. A distinct, tissue-specific microbiome dominated by the bacterial families Dietziaceae, Pseudomonadaceae and Oxalobacteraceae was observed in bile duct tissues. Systemic perturbation of the microbiome was noted in tumor and paired normal samples (vs non-cancer normals) for several bacterial families with a significant increase in Stenotrophomonas species distinguishing tumors vs paired normals. Comparison of parasite associated (OVa) vs non-associated (non-OVa) groups identified enrichment for specific enteric bacteria (Bifidobacteriaceae, Enterobacteriaceae and Enterococcaceae). One of the enriched families, Bifidobacteriaceae, was found to be dominant in the O. viverrini microbiome, providing a mechanistic link to the parasite. Functional analysis and comparison of CCA microbiomes revealed higher potential for producing bile acids and ammonia in OVa tissues, linking the altered microbiota to carcinogenesis. These results define how the unique microbial communities resident in the bile duct, parasitic infections and the tissue microenvironment can influence each other, and contribute to cancer
การเพิ่มประสิทธิภาพในกระบวนการสอบเทียบข้อมูลเครื่องมือวัด ภายในบริษัท กรณีศึกษา บริษัท อัลไลแอนซ์ ลอนดรี้ (ประเทศไทย) จำกัด
Get PDFงานวิจัยนี้มีวัตถุประสงค์เพื่อศึกษา 1) กระบวนการตรวจเช็กรหัสข้อมูลเครื่องมือวัด 2) วิธีการปรับปรุงขั้นตอนการปฏิบัติงานให้มีประสิทธิภาพ 3) วิธีการเพิ่มประสิทธิภาพในกระบวนการสอบเทียบข้อมูลเครื่องมือวัดภายในบริษัท จากการศึกษาขั้นตอนการตรวจเช็กรหัสข้อมูลเครื่องมือวัด พบว่าการตรวจเช็กข้อมูลเครื่องมือวัดมีความล่าช้าและใช้เวลาในการค้นหารหัสของแต่ละเครื่องมือจำนวนมาก จึงได้นำเทคนิคการวิเคราะห์ปัญหาด้วยหลักการ ECRS เข้ามาช่วยในการแก้ไขปัญหาและจัดทำคู่มือการใช้งานระบบการตรวจเช็กข้อมูลเครื่องมือวัด กระบวนการตรวจเช็กข้อมูลเครื่องมือวัดมีเวลาการทำงานเฉลี่ย เท่ากับ 1,496.57 วินาที ซึ่งลดลงจากเดิมคิดเป็นร้อยละ 24.94 กระบวนการตรวจเช็กข้อมูลเครื่องมือวัด พบว่าการตรวจเช็กข้อมูลเครื่องมือวัดดำเนินการล่าช้ากว่าที่กำหนด จึงได้นำหลักการลดความสูญเปล่า เพื่อปรับปรุงขั้นตอนการทำงานในกระบวนการตรวจเช็กข้อมูลเครื่องมือวัดให้สอดคล้องกับการนำระบบตรวจเช็กข้อมูลเครื่องมือวัดเข้ามาปรับใช้ โดยผลจากการปรับปรุงพบว่าขั้นตอนการตรวจเช็กข้อมูลเครื่องมือวัดลดลงจาก 7 ขั้นตอน เหลือเพียง 3 ขั้นตอน เวลาที่ใช้ในการทำงานลดลงจาก 3,375.63 วินาที เหลือ 1,496.57 วินาที ลดลงจากเดิม 1,879.06 วินาที หรือร้อยละ 55.66This research was conducted with the objectives of 1) to study the code checking process of measuring instrument data, 2) to study how to improve the efficiency of operational procedures, 3) to study how to increase the efficiency of the calibration process of measuring instrument data within the company. From the study of the process of checking the measuring tool data code, It was found that checking the instrument data was delayed and it took a lot of time to find the code of each instrument. Therefore, the problem analysis technique with the ECRS principle has been applied to help solve the problem and to prepare a user manual for measuring instrument data checking system. It was also found that checking the measurement data was delayed more than expected. Therefore, the principle of reducing wastage has been applied. To improve the workflow in the process of checking the measuring instrument data in line with the implementation of the measuring instrument data checking system. As a result of the improvement, it was found that the process of checking measuring instrument data was reduced from 7 steps to only 3 steps, the time spent on work was reduced from 3,375.63 seconds to 1,496.57 seconds, a decrease from the original 1,879.06 seconds or 55.66 percent
