<?xml version="1.0" encoding="UTF-8"?> <!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2d1 20170631//EN" "JATS-journalpublishing1.dtd"> <ArticleSet> <Article> <Journal> <PublisherName>isfcppharmaspire</PublisherName> <JournalTitle>Pharmaspire</JournalTitle> <PISSN>C</PISSN> <EISSN>o</EISSN> <Volume-Issue>Volume 11, Issue 1</Volume-Issue> <PartNumber/> <IssueTopic>Multidisciplinary</IssueTopic> <IssueLanguage>English</IssueLanguage> <Season>January-March, 2019</Season> <SpecialIssue>N</SpecialIssue> <SupplementaryIssue>N</SupplementaryIssue> <IssueOA>Y</IssueOA> <PubDate> <Year>2022</Year> <Month>06</Month> <Day>14</Day> </PubDate> <ArticleType>Pharmaceutics</ArticleType> <ArticleTitle>Pharma additives of natural origin: A mini-review</ArticleTitle> <SubTitle/> <ArticleLanguage>English</ArticleLanguage> <ArticleOA>Y</ArticleOA> <FirstPage>10</FirstPage> <LastPage>13</LastPage> <AuthorList> <Author> <FirstName>Rishav</FirstName> <LastName>Gupta</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>N</CorrespondingAuthor> <ORCID/> <FirstName>Sharib Raza</FirstName> <LastName>Khan</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>Rohit</FirstName> <LastName>Bhatia</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> </Author> </AuthorList> <DOI/> <Abstract>In the present time, a large number of natural additives are being used in the manufacturing of pharmaceutical products. Their demand is consistently increasing day by day due to several advantages offered by them. They are easily available, cheap, and stable and have very low incidence of toxicity. They are basically of plant and animal origins. The plant derived gums and mucilages comply with many requirements of pharmaceutical additives as they are non-toxic, stable, easily available, and associated with less regulatory issues as compared to their synthetic counterpart and inexpensive; also these can be easily modified to meet the specific need. In this article, authors have summarized various pharmaceutical additives of natural origin with their description and pharmaceutical applications.</Abstract> <AbstractLanguage>English</AbstractLanguage> <Keywords>Additives, toxicity, gums, mucilages, volatile oils</Keywords> <URLs> <Abstract>https://isfcppharmaspire.com/ubijournal-v1copy/journals/abstract.php?article_id=13870&title=Pharma additives of natural origin: A mini-review</Abstract> </URLs> <References> <ReferencesarticleTitle>References</ReferencesarticleTitle> <ReferencesfirstPage>16</ReferencesfirstPage> <ReferenceslastPage>19</ReferenceslastPage> <References>1. Bhattacharya L, Schuber S, Sheehan C, William R. Excipients: Background/ introduction. In: Excipient Development for Pharmaceutical Biotechnology and Drug Delivery Systems. United States: CRC Press; 2006. 2. Wade A, Weller PJ. Handbook of Pharmaceutical Excipients. Vol. 11. London: Pharmaceutical Press; 1994. p. 426-8. 3. Dinesh MS. Natural gums and mucilage’s in NDDS: Applications and recent approaches. Int J Pharm Tech Res 2012;4:799-814. 4. Perepelkin KE. Polymeric materials of the future based on renewable plant resources and biotechnologies: Fibres, films, plastics. Fiber Chem 2005;37:417-30. 5. Bi Y, Sunada H, Yonezawa Y, Danjo K, Otsuka A, Iida K. Preparation and evaluation of a compressed tablet rapidly disintegrating in the oral cavity. Chem Pharm Bull (Tokyo) 1996;44:2121-7. 6. Girish K, Dhiren JP, Shah VD, Prajapati VC. Gums and mucilages: Versatile excipients for pharmaceutical formulations. Asian J Pharm Sci 2009;4:309-32. 7. Qadry JS. Shah CS. Pharmacognosy. Ahmedabad, India: B S Shah Prakashan; 2008. 8. Kokate CK, Purohit AP, Gokhale SB, editors. Pharmacognosy. 22nd ed. India: Nirali Prakashan; 2003. p. 133-66. 9. Prajapati VD, Jani GK, Moradiya NG, Randeria NP. Pharmaceutical applications of various natural gums, mucilages and their modified forms. Carbohydr Polym 2013;92:1685-99. 10. John GL, Declan MD, James EK. The use of agar as a novel filler for monolithic matrices produced using hot melt extrusion. Eur J Pharm Biopharm 2006;64:75-81. 11. Jain NK, Dixit VK. Studies on gums and their derivatives as binding agent. Indian J Pharm Sci 1988;50:113-4. 12. Owen SC, Raymond CR, Paul JS, Paul JW. Handbook of Pharmaceutical Excipients. United Kingdom: Pharmaceutical Press, The American Pharmaceutical Association. 2003. p. 654-6. 13. Odeku OA, Itiola OA. Evaluation of the effects of khaya gum on the mechanical and release properties of paracetamol tablets. Drug Dev Ind Pharm 2003;29:311-20. 14. Kulkarni GT, Gowthamrajan K, Rao GB. Evaluation of binding properties of selected natural mucilages. J Sci Ind Res 2002;61:529-32. 15. Antony PJ, Sanghavi NM. A new disintegrant for pharmaceutical dosage forms. Drug Dev Ind Pharm 1997;23:413-5. 16. Kulkarni GT, Gowthamarajan K, Rao G B, Suresh B. Evaluation of binding properties of Plantago ovata and Trigonella foenum-graecum mucilages. Indian Drugs 2002;39:422-5. 17. Kulkarni GT, Gowthamarajan K, Satish KM, Suresh B. Gums and Mucilages: Therapeutic and Pharmaceutical Applications. India: NISCAIR-CSIR; 2002. p. 10-7. 18. Jani GK, Shah DP, Jain VC. Evaluating mucilage from Aloe barbadensis Miller as a pharmaceutical excipient for sustained-release matrix tablets. Pharm Technol 2007;31:90-8. 19. Patel MM, Chauhan GM, Patel LD. Mucilage of Lepidium sativum Linn (Asario) and Ocimum canum Sims. (Bavchi) as emulgents. Indian J Hosp Pharm 1987;24:200-2 . 20. Canadian Agency for Drugs and Technologies in Health. Essential Oil Products for Disinfection: Clinical Effectiveness, Cost Effectiveness and Guidelines. Ottawa: Canadian Agency for Drugs and Technologies in Health; 2014. 21. Kumar T, Gupta SK, Prajapati MK, Tripathi DK, Sharma V, Jain P. Natural excipients: A review. Asian J Pharm Life Sci 2012;2:97-108. 22. Chatwal GR. Pharmaceutical Inorganic Chemistry. Vol. 1. Bangalore: Himalaya Publishing House; 2010. 23. Kibbe AH. Handbook of Pharmaceutical Excipients. Washington, DC: Pharmaceutical Press; 2000. 24. Hon DN. Cellulose and Its Derivatives: Structures, Reactions and Medical Uses. New York, USA: Marcel Dekker; 1996. 25. Andreopoulos AG, Trantali PA. Study of biopolymers as carriers for controlled release. J Macromol Sci 2002;41:559-78. 26. Conti S, Maggi L, Segale L, Machiste EO, Conte U, Grenier P, et al. Matrices containing NaCMC and HPMC 1. Dissolution performance characterization. Int J Pharm 2007;333:136-42. 27. Chen J, Du GC. Environment Friendly Material Production and Application. Beijing: Huaxue Gongye Chubanshe; 2002. p. 46. 28. Tuovinen L, Peltonen S, Jarvinen K. Drug release from starch-acetate films. J Control Release 2003;91:345-54. 29. Banks W, Muir DD. Structure and chemistry of the starch granule. In: Preiss J, editor. The Biochemistry of Plants. Vol. 3. New York: Academic Press; 1980. p. 321-69.</References> </References> </Journal> </Article> </ArticleSet>