{"id":{"repo_id":"sdstate","oai_identifier":"oai:openprairie.sdstate.edu:etd-2522"},"canonical_url":"https://search.dev.ndltd.org/etd/sdstate/oai:openprairie.sdstate.edu:etd-2522","repository":{"repo_id":"sdstate","name":"South Dakota State University","base_url":"https://openprairie.sdstate.edu/do/oai/"},"display":{"title":"Fortification and Estimation of Vitamin D₃ in Pasteurized Process Cheese","abstract":"<p>The objectives of this study were to develop a method for the estimation of vitamin D<sub>3</sub> in pasteurized Process cheese using HPLC, and to develop a technique for the fortification of pasteurized Process cheese with vitamin D<sub>3</sub>. The method for vitamin D<sub>3</sub> estimation utilized high temperature (70°C for 30 min), alkaline saponification followed by extraction of unsaponifiable matter using petroleum ether: diethyl ether mixture (90: 10 v/v). One-ml silica cartridges were used for intermediate sample clean-up before the extracts were injected into HPLC. The HPLC system included a C<sub>10</sub> liquid chromatographic column (4.6 mm i.d. x 15 cm, 5 μm particle size) with UV detection at 254 nm, mobile phase: methanol: acetonitrile (70:30 v/v), injection volume of 100 μI and a flow rate of 1-ml/min. The retention time for vitamin 0 3 was approximately 9 min. A standard curve was prepared for quantification of vitamin D<sub>3 </sub>in unknown samples. This curve was prepared by adding standard solutions, at six levels of vitamin D<sub>3</sub>, to approximately 5 g of unfortified Process cheese samples, which were analyzed using the above procedure. Analysis for each level of vitamin D<sub>3</sub> was replicated 5 times. The areas obtained in each case were adjusted for the area in the control (cheese with no added vitamin D<sub>3</sub>) and then plotted against known concentrations of vitamin D<sub>3</sub>. The r<sup>2</sup> obtained for the curve was 0.9722. In the second phase of the study, pasteurized Process cheeses were manufactured with vitamin 03 added at a level of 100 IU per serving (28 g). Vitamin fortificants were commercially available water and fat dispersible forms of vitamin D<sub>3</sub>. Suitable dilutions of fortificants were made and added in the cheese cooker with other ingredients. Fortified Process cheeses were evaluated for recovery of vitamin D<sub>3</sub> during cheese manufacture and distribution of vitamin D<sub>3</sub> in the cheese mass. It was found that there was no loss of vitamin D<sub>3</sub> during manufacture of Process cheese and vitamin D<sub>3</sub> was uniformly distributed in the cheeses. Fortified Process cheeses, stored at 21 to 29°C and 4 to 6°C, did not exhibit any loss in vitamin D<sub>3</sub> activity over a 5 mo time period. As Process cheeses are often used as food ingredients and are heat treated to high temperatures for considerable time, stability of vitamin D<sub>3</sub> under such circumstances was also studied. Twenty-five to thirty percent of vitamin D<sub>3</sub> was destroyed under severe heat treatment of 232°C for 5 min. Sensory analysis showed that added vitamin D<sub>3 </sub>did not exhibit any off-flavor to the Process cheeses.</p>","abstract_html":"&lt;p&gt;The objectives of this study were to develop a method for the estimation of vitamin D&lt;sub&gt;3&lt;/sub&gt; in pasteurized Process cheese using HPLC, and to develop a technique for the fortification of pasteurized Process cheese with vitamin D&lt;sub&gt;3&lt;/sub&gt;. The method for vitamin D&lt;sub&gt;3&lt;/sub&gt; estimation utilized high temperature (70°C for 30 min), alkaline saponification followed by extraction of unsaponifiable matter using petroleum ether: diethyl ether mixture (90: 10 v/v). One-ml silica cartridges were used for intermediate sample clean-up before the extracts were injected into HPLC. The HPLC system included a C&lt;sub&gt;10&lt;/sub&gt; liquid chromatographic column (4.6 mm i.d. x 15 cm, 5 μm particle size) with UV detection at 254 nm, mobile phase: methanol: acetonitrile (70:30 v/v), injection volume of 100 μI and a flow rate of 1-ml/min. The retention time for vitamin 0 3 was approximately 9 min. A standard curve was prepared for quantification of vitamin D&lt;sub&gt;3 &lt;/sub&gt;in unknown samples. This curve was prepared by adding standard solutions, at six levels of vitamin D&lt;sub&gt;3&lt;/sub&gt;, to approximately 5 g of unfortified Process cheese samples, which were analyzed using the above procedure. Analysis for each level of vitamin D&lt;sub&gt;3&lt;/sub&gt; was replicated 5 times. The areas obtained in each case were adjusted for the area in the control (cheese with no added vitamin D&lt;sub&gt;3&lt;/sub&gt;) and then plotted against known concentrations of vitamin D&lt;sub&gt;3&lt;/sub&gt;. The r&lt;sup&gt;2&lt;/sup&gt; obtained for the curve was 0.9722. In the second phase of the study, pasteurized Process cheeses were manufactured with vitamin 03 added at a level of 100 IU per serving (28 g). Vitamin fortificants were commercially available water and fat dispersible forms of vitamin D&lt;sub&gt;3&lt;/sub&gt;. Suitable dilutions of fortificants were made and added in the cheese cooker with other ingredients. Fortified Process cheeses were evaluated for recovery of vitamin D&lt;sub&gt;3&lt;/sub&gt; during cheese manufacture and distribution of vitamin D&lt;sub&gt;3&lt;/sub&gt; in the cheese mass. It was found that there was no loss of vitamin D&lt;sub&gt;3&lt;/sub&gt; during manufacture of Process cheese and vitamin D&lt;sub&gt;3&lt;/sub&gt; was uniformly distributed in the cheeses. Fortified Process cheeses, stored at 21 to 29°C and 4 to 6°C, did not exhibit any loss in vitamin D&lt;sub&gt;3&lt;/sub&gt; activity over a 5 mo time period. As Process cheeses are often used as food ingredients and are heat treated to high temperatures for considerable time, stability of vitamin D&lt;sub&gt;3&lt;/sub&gt; under such circumstances was also studied. Twenty-five to thirty percent of vitamin D&lt;sub&gt;3&lt;/sub&gt; was destroyed under severe heat treatment of 232°C for 5 min. Sensory analysis showed that added vitamin D&lt;sub&gt;3 &lt;/sub&gt;did not exhibit any off-flavor to the Process cheeses.&lt;/p&gt;","abstract_has_math":false,"creators":["Upreti, Praveen"],"institution":null,"degree_name":"Master of Science (MS)","degree_level":"Thesis - University Access Only","degree_discipline":"Dairy Science","degree_department":null,"school":null,"contributors":["Vikram V. Mistry"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2001,"date_issued":"2001-01-01T08:00:00Z","date_published":"2001-01-01T08:00:00Z","updated_at":"2026-07-24T04:29:15Z","subjects":["Dairy Science"],"languages":["en"],"rights":["<p>In Copyright - Non-Commercial Use Permitted<br /><a href=\"http://rightsstatements.org/vocab/InC-NC/1.0/\">http://rightsstatements.org/vocab/InC-NC/1.0/</a></p>"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://openprairie.sdstate.edu/etd/1511","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Vikram V. 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The method for vitamin D<sub>3</sub> estimation utilized high temperature (70°C for 30 min), alkaline saponification followed by extraction of unsaponifiable matter using petroleum ether: diethyl ether mixture (90: 10 v/v). One-ml silica cartridges were used for intermediate sample clean-up before the extracts were injected into HPLC. The HPLC system included a C<sub>10</sub> liquid chromatographic column (4.6 mm i.d. x 15 cm, 5 μm particle size) with UV detection at 254 nm, mobile phase: methanol: acetonitrile (70:30 v/v), injection volume of 100 μI and a flow rate of 1-ml/min. The retention time for vitamin 0 3 was approximately 9 min. A standard curve was prepared for quantification of vitamin D<sub>3 </sub>in unknown samples. This curve was prepared by adding standard solutions, at six levels of vitamin D<sub>3</sub>, to approximately 5 g of unfortified Process cheese samples, which were analyzed using the above procedure. Analysis for each level of vitamin D<sub>3</sub> was replicated 5 times. The areas obtained in each case were adjusted for the area in the control (cheese with no added vitamin D<sub>3</sub>) and then plotted against known concentrations of vitamin D<sub>3</sub>. The r<sup>2</sup> obtained for the curve was 0.9722. In the second phase of the study, pasteurized Process cheeses were manufactured with vitamin 03 added at a level of 100 IU per serving (28 g). Vitamin fortificants were commercially available water and fat dispersible forms of vitamin D<sub>3</sub>. Suitable dilutions of fortificants were made and added in the cheese cooker with other ingredients. Fortified Process cheeses were evaluated for recovery of vitamin D<sub>3</sub> during cheese manufacture and distribution of vitamin D<sub>3</sub> in the cheese mass. It was found that there was no loss of vitamin D<sub>3</sub> during manufacture of Process cheese and vitamin D<sub>3</sub> was uniformly distributed in the cheeses. Fortified Process cheeses, stored at 21 to 29°C and 4 to 6°C, did not exhibit any loss in vitamin D<sub>3</sub> activity over a 5 mo time period. As Process cheeses are often used as food ingredients and are heat treated to high temperatures for considerable time, stability of vitamin D<sub>3</sub> under such circumstances was also studied. Twenty-five to thirty percent of vitamin D<sub>3</sub> was destroyed under severe heat treatment of 232°C for 5 min. Sensory analysis showed that added vitamin D<sub>3 </sub>did not exhibit any off-flavor to the Process cheeses.</p>"]},{"key":"dc:title","label":"Title","values":["Fortification and Estimation of Vitamin D₃ in Pasteurized Process Cheese"]}]}],"canonical_facts":{"dc:contributor":["Vikram V. Mistry"],"dc:creator":["Upreti, Praveen"],"dc:date.available":["2017-08-11T07:00:00Z"],"dc:description.abstract":["<p>The objectives of this study were to develop a method for the estimation of vitamin D<sub>3</sub> in pasteurized Process cheese using HPLC, and to develop a technique for the fortification of pasteurized Process cheese with vitamin D<sub>3</sub>. The method for vitamin D<sub>3</sub> estimation utilized high temperature (70°C for 30 min), alkaline saponification followed by extraction of unsaponifiable matter using petroleum ether: diethyl ether mixture (90: 10 v/v). One-ml silica cartridges were used for intermediate sample clean-up before the extracts were injected into HPLC. The HPLC system included a C<sub>10</sub> liquid chromatographic column (4.6 mm i.d. x 15 cm, 5 μm particle size) with UV detection at 254 nm, mobile phase: methanol: acetonitrile (70:30 v/v), injection volume of 100 μI and a flow rate of 1-ml/min. The retention time for vitamin 0 3 was approximately 9 min. A standard curve was prepared for quantification of vitamin D<sub>3 </sub>in unknown samples. This curve was prepared by adding standard solutions, at six levels of vitamin D<sub>3</sub>, to approximately 5 g of unfortified Process cheese samples, which were analyzed using the above procedure. Analysis for each level of vitamin D<sub>3</sub> was replicated 5 times. The areas obtained in each case were adjusted for the area in the control (cheese with no added vitamin D<sub>3</sub>) and then plotted against known concentrations of vitamin D<sub>3</sub>. The r<sup>2</sup> obtained for the curve was 0.9722. In the second phase of the study, pasteurized Process cheeses were manufactured with vitamin 03 added at a level of 100 IU per serving (28 g). Vitamin fortificants were commercially available water and fat dispersible forms of vitamin D<sub>3</sub>. Suitable dilutions of fortificants were made and added in the cheese cooker with other ingredients. Fortified Process cheeses were evaluated for recovery of vitamin D<sub>3</sub> during cheese manufacture and distribution of vitamin D<sub>3</sub> in the cheese mass. It was found that there was no loss of vitamin D<sub>3</sub> during manufacture of Process cheese and vitamin D<sub>3</sub> was uniformly distributed in the cheeses. Fortified Process cheeses, stored at 21 to 29°C and 4 to 6°C, did not exhibit any loss in vitamin D<sub>3</sub> activity over a 5 mo time period. As Process cheeses are often used as food ingredients and are heat treated to high temperatures for considerable time, stability of vitamin D<sub>3</sub> under such circumstances was also studied. Twenty-five to thirty percent of vitamin D<sub>3</sub> was destroyed under severe heat treatment of 232°C for 5 min. Sensory analysis showed that added vitamin D<sub>3 </sub>did not exhibit any off-flavor to the Process cheeses.</p>"],"dc:identifier":["https://openprairie.sdstate.edu/etd/1511"],"dc:language":["en"],"dc:rights":["<p>In Copyright - Non-Commercial Use Permitted<br /><a href=\"http://rightsstatements.org/vocab/InC-NC/1.0/\">http://rightsstatements.org/vocab/InC-NC/1.0/</a></p>"],"dc:subject":["Dairy Science"],"dc:title":["Fortification and Estimation of Vitamin D₃ in Pasteurized Process Cheese"],"thesis:degree_discipline":["Dairy Science"],"thesis:degree_level":["Thesis - University Access Only"],"thesis:degree_name":["Master of Science (MS)"]},"updated_at":"2026-07-24T04:29:15Z"}