{"id":18634,"date":"2024-11-26T08:00:48","date_gmt":"2024-11-26T08:00:48","guid":{"rendered":"https:\/\/www.thermofisher.com\/blog\/behindthebench\/?p=18634"},"modified":"2024-12-05T20:06:22","modified_gmt":"2024-12-05T20:06:22","slug":"should-uv-vis-be-used-to-confirm-the-quality-of-ibuprofen","status":"publish","type":"post","link":"https:\/\/www.thermofisher.com\/blog\/behindthebench\/should-uv-vis-be-used-to-confirm-the-quality-of-ibuprofen\/","title":{"rendered":"Should UV-Vis be used to Confirm the Quality of Ibuprofen?"},"content":{"rendered":"<p>Ibuprofen, a widely used medication for treating pain, fever, and inflammation, is an active pharmaceutical ingredient (API) whose quality must be rigorously controlled. The United States Pharmacopeia (USP) and European Pharmacopoeia (EP) have developed detailed written reports \u2013 referred to as monographs \u2013 that outline specific identification tests, procedures, and acceptance criteria to ensure the strength, quality, and purity of ibuprofen.<\/p>\n<p>Spectrophotometric tests are crucial to confirming the identity and testing the purity of ibuprofen samples in <a href=\"https:\/\/www.thermofisher.com\/us\/en\/home\/industrial\/manufacturing-processing\/improving-pharmaceutical-biotech-manufacturing-processes-production-methods\/technologies.html?icid=CAD_blog_LSM_2024Nov#uv-visible-spectroscopy\">pharmaceutical quality control laboratories<\/a>, so these monographs contain detailed instructions utilizing a variety of analytical instrumentation used in the testing.\u00a0 The various analytical techniques include infrared absorption spectroscopy, ultraviolet-visible (UV-Vis) spectroscopy, melting point analysis, and chromatography.<\/p>\n<p>The spectrophotometric ibuprofen identification test according to the EP ibuprofen monograph requires measuring a test sample and comparing the ratios of its absorbance values to confirm they are within an acceptable range. We took a look at the use of UV-Vis spectrophotometers to perform the essential identification tests for ibuprofen as described in the USP and EP monographs, and have outlined below the tests we performed and the results.<\/p>\n<h2>What is UV-Vis<\/h2>\n<p>UV-Vis, or Ultraviolet-Visible Spectroscopy, is a non-destructive analytical technique used to measure the absorbance or reflectance of a sample in the ultraviolet and visible regions of the electromagnetic spectrum. The technique is commonly employed to determine the concentration of a substance in solution, analyze the purity of compounds, and study the electronic transitions in molecules.<\/p>\n<p>In UV-Vis spectroscopy, a sample is exposed to light in the UV (typically 200-400 nm) and visible (typically 400-700 nm) wavelength ranges. The instrument measures the intensity of light before and after it passes through the sample. These intensities can be used to calculate absorbance as the loss of light intensity as it passes through a sample arises from the absorption of photons,. According to <a href=\"https:\/\/chem.libretexts.org\/Bookshelves\/Physical_and_Theoretical_Chemistry_Textbook_Maps\/Supplemental_Modules_(Physical_and_Theoretical_Chemistry)\/Spectroscopy\/Electronic_Spectroscopy\/Electronic_Spectroscopy_Basics\/The_Beer-Lambert_Law\">Beer-Lambert&#8217;s law<\/a>, a linear relationship exists between absorbance and analyte concentration.<\/p>\n<h2>Testing with UV-Vis<\/h2>\n<p>The identification tests for ibuprofen were carried out using a <a href=\"https:\/\/www.thermofisher.com\/us\/en\/home\/industrial\/spectroscopy-elemental-isotope-analysis\/molecular-spectroscopy\/uv-vis-spectrophotometry.html?icid=CAD_blog_LSM_2024Nov\">UV-Vis spectrophotometer.<\/a> The procedure involved comparing the absorbance spectra of a test sample of ibuprofen against a standard ibuprofen sample. The USP and EP monographs provide specific instructions on how these tests should be conducted.<\/p>\n<ol>\n<li><strong>USP Identification Test:<\/strong><\/li>\n<\/ol>\n<ul>\n<li>The identity of the ibuprofen test sample was confirmed by comparing its absorbance spectrum to that of a standard ibuprofen sample.<\/li>\n<li>The absorbance peaks at specific wavelengths were matched to ensure the sample met the USP criteria.<\/li>\n<\/ul>\n<ol>\n<li><strong>EP Identification Test:<\/strong><\/li>\n<\/ol>\n<ul>\n<li>The test involved visual inspection and comparison of absorbance ratios at designated wavelengths.<\/li>\n<li>The absorbance ratios of the test sample were compared to those specified in the EP monograph to confirm the sample\u2019s identity.<\/li>\n<\/ul>\n<p><strong>Results:<\/strong><\/p>\n<p>The UV-Vis spectrophotometric tests successfully identified the ibuprofen test samples according to both USP and EP requirements. The absorbance spectra and ratios matched the criteria outlined in the respective monographs, confirming the identity and quality of the ibuprofen samples.<\/p>\n<p><strong>Conclusion:<\/strong><\/p>\n<p><a href=\"https:\/\/www.thermofisher.com\/us\/en\/home\/industrial\/spectroscopy-elemental-isotope-analysis\/molecular-spectroscopy\/uv-vis-spectrophotometry.html?icid=CAD_blog_LSM_2024Nov\">UV-Vis spectrophotometers<\/a> are essential analytical instruments for pharmaceutical quality control laboratories. They provide a reliable and efficient means of performing spectrophotometric identification tests for ibuprofen, as required by USP and EP monographs. The successful application of these tests ensures that ibuprofen samples conform to the stringent standards for strength, quality, and purity, thereby safeguarding public health.<\/p>\n<h2>Summary<\/h2>\n<p>UV-Vis spectrophotometry can play a critical role in pharmaceutical quality control, particularly in the identification and verification of ibuprofen samples. By adhering to the detailed procedures and acceptance criteria outlined in the USP and EP monographs, laboratories can ensure the integrity and efficacy of ibuprofen as a therapeutic agent.<\/p>\n<p>For more specific information, download the application note: <a href=\"https:\/\/assets.thermofisher.com\/TFS-Assets%2FMSD%2FApplication-Notes%2FAN53349-spectrophotometric-analysis-ibuprofen.pdf?icid=CAD_blog_LSM_2024Nov\"><em>Spectrophotometric Analysis of Ibuprofen According to USP and EP Monographs<\/em><\/a><em>.<\/em><\/p>\n<h2>References:<\/h2>\n<ol>\n<li>United States Pharmacopeia and National Formulary (USP 43-NF 38), Monographs, Ibuprofen.<\/li>\n<li>European Pharmacopeia (EP 9.6), Monographs, Ibuprofen.<\/li>\n<\/ol>\n<ul>\n<li>Application note: <a href=\"https:\/\/assets.thermofisher.com\/TFS-Assets%2FMSD%2FApplication-Notes%2FAN53349-spectrophotometric-analysis-ibuprofen.pdf?icid=CAD_blog_LSM_2024Nov\"><em>Spectrophotometric Analysis of Ibuprofen According to USP and EP Monographs<\/em><\/a><em>.<\/em><\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Ibuprofen, a widely used medication for treating pain, fever, and inflammation, is an active pharmaceutical ingredient (API) whose quality must be rigorously controlled. The United States Pharmacopeia (USP) and European Pharmacopoeia (EP) have developed detailed written reports \u2013 referred to as monographs \u2013 that outline specific identification tests, procedures, and acceptance criteria to ensure the<\/p>\n","protected":false},"author":120,"featured_media":18635,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_kad_blocks_custom_css":"","_kad_blocks_head_custom_js":"","_kad_blocks_body_custom_js":"","_kad_blocks_footer_custom_js":"","_monsterinsights_skip_tracking":false,"_genesis_hide_title":false,"_genesis_hide_breadcrumbs":false,"_genesis_hide_singular_image":false,"_genesis_hide_footer_widgets":false,"_genesis_custom_body_class":"","_genesis_custom_post_class":"","_genesis_layout":"","_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":""},"categories":[1087],"tags":[2442,2327,2349,2441,2363],"division":[],"class_list":{"0":"post-18634","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-pharmamfg","8":"tag-ibuprofen-manufacturing","9":"tag-pharma-manufacturing","10":"tag-pharmaceutical-quality","11":"tag-pill-manufacturing","12":"tag-uv-vis-spectroscopy","13":"entry"},"_selected_authors":"","_selected_reviewers":"","acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v27.8 (Yoast SEO v27.8) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Should UV-Vis be used to Confirm the Quality of Ibuprofen? - Behind the Bench<\/title>\n<meta name=\"description\" content=\"We compared a UV-Vis spectrophotometer absorbance spectra from an ibuprofen test sample against a standard ibuprofen sample. 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Analytical testing plays a critical role in verifying product identity, composition, and consistency. Among modern analytical techniques, Raman spectroscopy stands out as a powerful\u2026","rel":"","context":"In &quot;General&quot;","block_context":{"text":"General","link":"https:\/\/admin.acceleratingscience.com\/behindthebench\/general\/"},"img":{"alt_text":"Syringes, injection bottles and tablets lying on the table. Close-up, indoors, view from above. Day light, studio photo. 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Drug candidates are more complex, development timelines are tighter, and expectations for quality and consistency continue to rise. Against this backdrop, one question comes up repeatedly for formulation and manufacturing teams:\u00a0should we scale up, or should we scale\u2026","rel":"","context":"In &quot;General&quot;","block_context":{"text":"General","link":"https:\/\/admin.acceleratingscience.com\/behindthebench\/general\/"},"img":{"alt_text":"Sorting pharmaceutical capsules by a sorting machine on a production line","src":"https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/01\/iStock-1499814881.jpg?resize=350%2C200&ssl=1","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/01\/iStock-1499814881.jpg?resize=350%2C200&ssl=1 1x, https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/01\/iStock-1499814881.jpg?resize=525%2C300&ssl=1 1.5x, https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/01\/iStock-1499814881.jpg?resize=700%2C400&ssl=1 2x, https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/01\/iStock-1499814881.jpg?resize=1050%2C600&ssl=1 3x, https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/01\/iStock-1499814881.jpg?resize=1400%2C800&ssl=1 4x"},"classes":[]},{"id":19658,"url":"https:\/\/www.thermofisher.com\/blog\/behindthebench\/is-raman-spectroscopy-a-better-verification-method-in-pharmaceutical-manufacturing\/","url_meta":{"origin":18634,"position":2},"title":"Is Raman Spectroscopy a Better Verification Method in Pharmaceutical Manufacturing?","author":"Marlene Gasdia-Cochrane","date":"May 5, 2026","format":false,"excerpt":"Article Summary Verification testing is a critical step in pharmaceutical manufacturing, helping to ensure that every product released meets strict safety, quality, and regulatory standards. Verification helps ensure that products contain the correct active ingredients, meet concentration specifications, are free from contamination, and maintain structural and chemical integrity. This process\u2026","rel":"","context":"In &quot;Pharma &amp; Biotech Manufacturing&quot;","block_context":{"text":"Pharma &amp; Biotech Manufacturing","link":"https:\/\/admin.acceleratingscience.com\/behindthebench\/pharmamfg\/"},"img":{"alt_text":"Yellow pill and red check mark sitting on brown wood surface in front of abstract defocused background. Horizontal composition with selective focus and copy space. Front view. 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While traditional manufacturing focuses on larger equipment and higher throughput, many specialized pharmaceutical programs utilize continuous manufacturing and face different constraints. In these cases, successful scale-up is measured by maintaining process consistency, reproducibility, and control rather than\u2026","rel":"","context":"In &quot;Pharma &amp; Biotech Manufacturing&quot;","block_context":{"text":"Pharma &amp; Biotech Manufacturing","link":"https:\/\/admin.acceleratingscience.com\/behindthebench\/pharmamfg\/"},"img":{"alt_text":"A pill on blue background","src":"https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/06\/iStock-1218800138.jpg?resize=350%2C200&ssl=1","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/06\/iStock-1218800138.jpg?resize=350%2C200&ssl=1 1x, https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/06\/iStock-1218800138.jpg?resize=525%2C300&ssl=1 1.5x, https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/06\/iStock-1218800138.jpg?resize=700%2C400&ssl=1 2x, https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/06\/iStock-1218800138.jpg?resize=1050%2C600&ssl=1 3x, https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/06\/iStock-1218800138.jpg?resize=1400%2C800&ssl=1 4x"},"classes":[]},{"id":19376,"url":"https:\/\/www.thermofisher.com\/blog\/behindthebench\/why-most-modern-drug-candidates-fail-at-solubility\/","url_meta":{"origin":18634,"position":4},"title":"Why Most Modern Drug Candidates Fail at Solubility\u00a0","author":"Marlene Gasdia-Cochrane","date":"February 17, 2026","format":false,"excerpt":"Drug discovery capabilities continue to advance rapidly. Medicinal chemists are designing molecules with unprecedented potency and selectivity, enabling therapies that were not possible even a decade ago. Yet despite these scientific gains, many promising drug candidates still struggle to reach patients. One of the most common reasons is poor solubility.\u00a0\u2026","rel":"","context":"In &quot;General&quot;","block_context":{"text":"General","link":"https:\/\/admin.acceleratingscience.com\/behindthebench\/general\/"},"img":{"alt_text":"Fizzing Tablet in Water","src":"https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/01\/iStock-182713597.jpg?resize=350%2C200&ssl=1","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/01\/iStock-182713597.jpg?resize=350%2C200&ssl=1 1x, https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/01\/iStock-182713597.jpg?resize=525%2C300&ssl=1 1.5x, https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/01\/iStock-182713597.jpg?resize=700%2C400&ssl=1 2x, https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/01\/iStock-182713597.jpg?resize=1050%2C600&ssl=1 3x, https:\/\/i0.wp.com\/admin.acceleratingscience.com\/behindthebench\/wp-content\/uploads\/sites\/9\/2026\/01\/iStock-182713597.jpg?resize=1400%2C800&ssl=1 4x"},"classes":[]},{"id":19528,"url":"https:\/\/www.thermofisher.com\/blog\/behindthebench\/geometry-dependent-vs-parameter-driven-scale-up-in-pharmaceutical-manufacturing\/","url_meta":{"origin":18634,"position":5},"title":"Geometry-Dependent\u00a0vs\u00a0Parameter-Driven Scale Up\u00a0in Pharmaceutical Manufacturing\u00a0","author":"Marlene Gasdia-Cochrane","date":"March 31, 2026","format":false,"excerpt":"Overview\u00a0 Scale-up challenges in pharmaceutical manufacturing often stem from a fundamental distinction between geometry-dependent and parameter-driven systems. Processes that perform consistently at lab scale can shift unexpectedly at production scale. This is\u00a0often because the\u00a0governing physical logic was misunderstood. In geometry-dependent systems, equipment size directly alters heat transfer, mixing, dwell time,\u2026","rel":"","context":"In &quot;Pharma &amp; Biotech Manufacturing&quot;","block_context":{"text":"Pharma &amp; Biotech Manufacturing","link":"https:\/\/admin.acceleratingscience.com\/behindthebench\/pharmamfg\/"},"img":{"alt_text":"Macro Shot of Pink Pills During Production and Packing Process on Modern Pharmaceutical Factory. 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