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    DEVELOPMENT OF SORBITAN MONOSTEARATE ORGANOGELS FOR CONTROLLED DELIVERY SYSTEMS A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF Bachelor of Technology (Biomedical Engineering) Submitted By MEENAKSHI SINGH Roll No. 107BM008 Under the Guidance of Dr. Kunal Pal Department of Biotechnology & Medical Engineering National Institute of Technology Rourkela 769008 DEPARTMENT OF BIOTECHNOLOGY & MEDICAL ENGINEERING‚ NATIONAL INSTITUTE OF TECHNOLOGY-ROURKELA

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    shampoos‚ bubble baths‚ facial scrubs etc. • Stabilised emulsions - moisterisers‚ sunscreens etc. • Concealer products - make up • Alcoholic and hydroalcoholic solutions - colognes‚ toners‚ aftershaves etc. • Alcoholic and hydroalcoholic gels - hair gels‚ fragrance gels • Solid wax products - lipsticks. leg wax etc. INTRODUCTION Cosmetic manufacturing in New Zealand is a fairly simple industry‚ with manufacturing being limited mainly to blending and packaging. Few of the ingredients are made in New Zealand

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    SYNTHESIS AND CHARACTERIZATION OF HIGHLY CROSSLINKED HYALURONAN HYDROGELS Newell R. Washburn1‚ Sidi A. Bencherif1‚ Abiraman Srinivasan2‚ Jeffrey O. Hollinger2‚ Ferenc Horkay3‚ Krzysztof Matyjaszewski1 Departments of 1Chemistry and 2Biomedical Engineering Carnegie Mellon University‚ Pittsburgh‚ PA 15213 3 Laboratory of Integrative and Medical Biophysics National Institutes of Health‚ NICHD 13 South Drive‚ Bethesda‚ MD 20892 Introduction Methacrylation of hyaluronic acid (HA) with glycidyl methacrylate

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    Gel Manicures

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    Marissa Arias Senior Rhetoric Graf-8 April 14‚ 2014 Gel II Manicure Many women and even some men love to get their nails done‚ but hate how much time it takes to dry and on top of that they are extremely easy to ruin and chip. There is a new type of manicure trending know as Shellac‚ Gel nails‚ or No chip. According to my cosmetology instructor Samantha Rudman‚ this process takes about 35 to 40 minutes but dries in seconds. Many individuals would love to know this process even the men that

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    Agarose gel

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    Agarose Gel Electophoresis of DNA Topoisomers Introduction DNA can exist as different isomers that change the confirmation of the DNA’s structure. DNA can be in a linear confirmation this is a relaxed confirmation as the DNA can rotate about its axis unconstrained. It can also exist as a nicked circle this is also a relaxed confirmation as the DNA strands can again rotate freely with respect to one another. Covalently closed circular DNA or cccDNA exists as a supercoil this is because the covalent

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    Irish Gel

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    Distribution in many ways: * Online sales * Traditional stores * Selling to spas * Wholesalers * Pharmacies 2. Secure ingredient wholesaler from China. Establish from 2 to 4 products In order to increase sales Irish breeze shower gel could be linked to other company’s products (wipes‚ baby care). It would significantly reduce marketing costs as well as in the retail environment‚ the company is committed to driving sales‚ especially in the supermarket channel‚ by providing high

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    Gel Electrophoresis

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    Laura Gallagher Partner: Rob Einersen Biology Period D Mr. Alvarez 15 February 2013 Gel Electrophoresis Introduction: Agarose Gel Electrophoresis is a process in which the process of determining whether a strand of DNA is either positively or negatively charged. The container in which the gel is stored has a negative and positive side; whichever side the DNA molecules go to means the DNA is charged the opposite way. (Ware‚ Lunte‚ Gardiner)For example if a DNA molecule

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    Gel Filtration

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    Gel filtration GEL FILTRATION OF PROTIENS Aim: The aim of this experiment is to identify proteins from a complex mixture using the gel filtration technique also known as size exclusion chromatography. This technique is widely used by biochemists when proteins larger than the pores are excluded from the column and the smaller molecules elute last and then collected in test tubes for examination by spectroscopic techniques. The red/brown proteins‚ in particular‚ will be observed closely

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    FLVS 9.07 Live Lesson

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    Blackboard Collaborate ?? LIVE LESSON 9.07 V14 Slide1 Page 1. Oct 16‚ 2013 4:58:28 PM Blackboard Collaborate ?? LIVE LESSON 9.07 V14 Slide2 Page 2. Oct 16‚ 2013 4:58:28 PM Blackboard Collaborate ?? LIVE LESSON 9.07 V14 Oct 16‚ 2013 4:58:28 PM Common Core Standards Covered in this Lesson: Page 3. Blackboard Collaborate ?? LIVE LESSON 9.07 V14 Slide4 Page 4. Oct 16‚ 2013 4:58:28 PM Blackboard Collaborate ?? LIVE LESSON 9.07 V14 Students Page 5. Oct

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    SDS-PAGE

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    SDS-PAGE Laboratory Summary Electrophoresis is a technique where molecules are separated according to their physical properties such as size‚ charge‚ and/or shape. Charged proteins are commonly separated in this matter using PAGE (polyacrylamide gel electrophoresis) to identify individual proteins present in samples. In this lab‚ SDS-PAGE was used. SDS-PAGE separates charged proteins primarily by size because the ionic detergent sodium dodecyl sulfate (SDS) with 2-mercaptoethanol disassociates

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