<?xml version="1.0"?>
<xml><ArticleSet><Article><Journal><PublisherName>Radiance Research Academy</PublisherName><JournalTitle>International Journal of Current Research and Review</JournalTitle><PISSN>2231-2196</PISSN><EISSN>0975-5241</EISSN><Volume>16</Volume><Issue>22</Issue><IssueLanguage>English</IssueLanguage><SpecialIssue>N</SpecialIssue><PubDate><Year>2024</Year><Month>November</Month><Day>27</Day></PubDate></Journal><ArticleType>Healthcare</ArticleType><ArticleTitle>&#xD;
	Effects of Active School Transportation on Physical Fitness of Congolese Intellectual Disabilities Adolescents&#xD;
&#xD;
&#xD;
&#xD;
	&#xA0;&#xD;
&#xD;
&#xD;
&#xD;
	&#xA0;&#xD;
&#xD;
&#xD;
&#xD;
	&#xA0;&#xD;
&#xD;
</ArticleTitle><ArticleLanguage>English</ArticleLanguage><FirstPage>01</FirstPage><LastPage>08</LastPage><AuthorList><Author>Mabounda Kounga Paul Roger</Author><AuthorLanguage>English</AuthorLanguage><Author> Boussana Alain Marc</Author><AuthorLanguage>English</AuthorLanguage><Author> Agbodjogbe Wilfrid Kpedetin Dieu-Donne</Author><AuthorLanguage>English</AuthorLanguage></AuthorList><Abstract>&#xD;
	Introduction: Adolescents with intellectual disabilities (ID) tend to have poorer physical fitness than their typically developing peers. Active transport provides substantial health benefits from increased physical activity. But few is known on the Congolese normal-weight and overweight with intellectual disabilities. Aim/Objectives: This study aimed to evaluate the effect of active school-home transportation on the physical fitness of Congolese adolescents with intellectual disability disorder. Methods: A total of 28 adolescents with mild and moderate intellectual disability, were divided into normal-weight with intellectual disabilities (NWID, n = 18, age) and overweight with intellectual disabilities (OWID, n = 10, age). Their physical fitness parameters were assessed at three periods: on April-June 2023 (T0), October-November (T1) and December 2023 (T2). The active transportation (walking) and period of rest effects on adolescent&#x2019;s physical fitness were assessed on T0/ T2 and T1 respectively. Physical fitness parameters were related to movement functionality (the test of balance) and health-related condition (waist circumference, 6-minute walk tests, push-up and sit-stand tests). Results: Waist circumference was significantly lowers (all p &lt; 0.05) among NWID and OWID at T0 and T2 periods than on the T1 period. NWID scored significantly higher in flexibility, balance, push-up, 6MWT and VO2max (all p &lt; 0.01) tests than OWID whereas OWID improve better the flexibility at the third period (p &gt; 0.05). Compared to the second period, NWID scored significantly higher in the T0 period for balance, push-up and VO2max (all p &lt; 0.05) and scored significantly higher in the T2 period for flexibility, balance, distance travel, push-up and VO2max (all p &lt; 0.05). Conclusion: Active transportation widely improved functionality and health related parameters of normal weight Congolese intellectual disabilities adolescents. School time periods exerted more effects on balance, flexibility, distance traveled, and cardiorespiratory fitness than the holyday on both normal weight and overweight groups.&#xD;
&#xD;
</Abstract><AbstractLanguage>English</AbstractLanguage><Keywords>Physical fitness, Active school transportation, Intellectual disability, Congolese, Adolescents, Health</Keywords><URLs><Abstract>http://ijcrr.com/abstract.php?article_id=4828</Abstract><Fulltext>http://ijcrr.com/article_html.php?did=4828</Fulltext></URLs><References></References></Article></ArticleSet><ArticleSet><Article><Journal><PublisherName>Radiance Research Academy</PublisherName><JournalTitle>International Journal of Current Research and Review</JournalTitle><PISSN>2231-2196</PISSN><EISSN>0975-5241</EISSN><Volume>16</Volume><Issue>22</Issue><IssueLanguage>English</IssueLanguage><SpecialIssue>N</SpecialIssue><PubDate><Year>2024</Year><Month>November</Month><Day>27</Day></PubDate></Journal><ArticleType>Healthcare</ArticleType><ArticleTitle>&#xD;
	A Holistic Review on Applications of Different Grades of Polyethylene oxide in Pharmaceutical Formulation Development&#xD;
&#xD;
&#xD;
&#xD;
	&#xA0;&#xD;
&#xD;
&#xD;
&#xD;
	&#xA0;&#xD;
&#xD;
</ArticleTitle><ArticleLanguage>English</ArticleLanguage><FirstPage>09</FirstPage><LastPage>17</LastPage><AuthorList><Author>Dinesh Kumar Das</Author><AuthorLanguage>English</AuthorLanguage><Author> Anjan Kumar</Author><AuthorLanguage>English</AuthorLanguage><Author> Ch Niranjan Patra</Author><AuthorLanguage>English</AuthorLanguage></AuthorList><Abstract>&#xD;
	Polyethylene oxide (PEO) is a multifaceted polymer with extensive applications in pharmaceutical product development. This review highlights its significant roles in various drug delivery systems. In hydrogels, PEO&#x2019;s hydrophilicity and gel-forming capabilities enhance drug stability and controlled release. Osmotic pumps benefit from PEO&#x2019;s ability to regulate osmotic pressure and drug solubility, ensuring precise and consistent drug delivery. PEO&#x2019;s mucoadhesive properties improve drug retention and bioavailability in mucoadhesive drug delivery systems, providing sustained therapeutic effects. In gastro-retentive drug delivery systems, PEO prolongs gastric residence time, enhancing the bioavailability of drugs absorbed primarily in the stomach. Finally, PEO&#x2019;s thermoplastic properties make it an essential component in hot melt extrusion processes, facilitating the formation of homogenous drug-polymer matrices and improving the solubility of poorly water-soluble drugs. Overall, PEO&#x2019;s versatility and effectiveness across these applications underscore its critical role in advancing pharmaceutical formulations and optimizing therapeutic&#xD;
&#xD;
</Abstract><AbstractLanguage>English</AbstractLanguage><Keywords>Hydrogel, Osmotic DDS, Mucoadhesive DDS, Gastro-retentive DDS, Hot-melt extrusion process and polyox</Keywords><URLs><Abstract>http://ijcrr.com/abstract.php?article_id=4829</Abstract><Fulltext>http://ijcrr.com/article_html.php?did=4829</Fulltext></URLs><References>&#xD;
	1. Hussain G, Al-Ghamdi K. PEO coating as lubrication means for SPIF of titanium sheet: characteristics and performance. Mater Res Innov 2014; 18 (2): 727-733.&#xD;
	2. Kim M, Vala M, Ertsgaard CT, Oh SH, Lodge TP, Bates J, et al. Surface plasmon resonance study of the binding of PEO&#x2013;PPO&#x2013; PEO triblock copolymer and PEO homopolymer to supported lipid bilayers. Langmuir 2018; 34 (23): 6703-6712.&#xD;
	3. Khan K, Hanif MB, Xin H, Hussain A, Ali HG, Fu B, et al. PEOBased Solid Composite Polymer Electrolyte for High Capacity Retention All?Solid?State Lithium Metal Battery. Small. 2024; 20 (4): 57-72.&#xD;
	4. Rivero D, Gouveia LM, M&#xFC;ller AJ, Saez AE. Shear-thickening behavior of high molecular weight poly (ethylene oxide) solutions. Rheologica Acta 2012; 51: 13-20.&#xD;
	5. Ahmed HT, Abdullah OG. Preparation and composition optimization of PEO: MC polymer blend films to enhance electrical conductivity. Polymers. 2019, 11 (5), 853.&#xD;
	6. Stringer JL, Peppas NA. Diffusion of small molecular weight drugs in radiation-crosslinked poly (ethylene oxide) hydrogels. Journal of Controlled Release (JCR). 1996; 42 (2): 195-202.&#xD;
	7. Bergstrand N, Edwards K. Effects of poly (ethylene oxide)&#x2013;poly (propylene oxide)&#x2013;poly (ethylene oxide) triblock copolymers on structure and stability of liposomal dioleoylphosphatidylethanolamine. J Colloid and Interface Sci. 2004; 276 (2): 400-407.&#xD;
	8. Crcarevska MS, Geskovski N, Calis S, Dimchevska S, Kuzmanovska S, Petrusevski G, et al. Definition of formulation design space, in vitro bioactivity and in vivo biodistribution for hydrophilic drug loaded PLGA/PEO&#x2013;PPO&#x2013;PEO nanoparticles using OFAT experiments. Eur J Pharm Sci. 2013; 49 (1): 65-80.&#xD;
	9. Kanjickal D, Lopina S, Evancho?Chapman MM, Schmidt S, Donovan D. Effects of sterilization on poly (ethylene glycol) hydrogels. J Biomed Mater Res Part A: An Official Journal of The Society for Biomaterials, The Japanese Society for Biomaterials, and The Australian Society for Biomaterials and the Korean Society for Biomaterials. 2008; 87 (3): 608-617.&#xD;
	10. Liaw J, Lin YC. Evaluation of poly (ethylene oxide)&#x2013;poly (propylene oxide)&#x2013;poly (ethylene oxide)(PEO&#x2013;PPO&#x2013;PEO) gels as a release vehicle for percutaneous fentanyl. Journal of Controlled Release (JCR). 2000; 68 (2): 273-282.&#xD;
	11. Emara LH, Taha NF, Badr RM, Mursi NM. Development of an osmotic pump system for controlled delivery of diclofenac sodium. Drug Discoveries &amp; Therapeutics. 2012; 6 (5): 269-277.&#xD;
	12. Wu C, Zhao Z, Zhao Y, Hao Y, Liu Y, Liu C. Preparation of a push&#x2013;pull osmotic pump of felodipine solubilized by mesoporous silica nanoparticles with a core&#x2013;shell structure. Inter J Pharm. 2014; 475 (1-2); 298-305.&#xD;
	13. Li Y, Pan H, Duan H, Chen J, Zhu Z, Fan J, et al. Double-layered osmotic pump controlled release tablets of actarit: In vitro and in vivo evaluation. Asian J Pharm Sci. 2019; 14 (3); 340-348.&#xD;
	14. Kumar P, Singh S, Mishra B. Development and evaluation of elementary osmotic pump of highly water-soluble drug: tramadol hydrochloride. Curr Drug Deliv. 2009; 6 (1): 130-139.&#xD;
	15. Lin W, Li Y, Shi Q, Liao X, Zeng Y, Tian W, et al. Preparation and evaluation of bilayer-core osmotic pump tablets contained topiramate. Plos One. 2022; 17 (2): e0264457.&#xD;
	16. Stie MB, G&#xE4;tke JR, Wan F, Chronakis IS, Jacobsen J, Nielsen HM. Swelling of mucoadhesive electrospun chitosan/polyethylene oxide nanofibers facilitates adhesion to the sublingual mucosa. Carbohydrate polymers. 2020; 242: 116-128.&#xD;
	17. Park JS, Oh YK, Yoon H, Kim JM, Kim CK. In situ gelling and mucoadhesive polymer vehicles for controlled intranasal delivery of plasmid DNA. Journal of Biomedical Materials Research: An Official Journal of The Society for Biomaterials and The Japanese Society for Biomaterials. 2002; 59 (1): 144-151.&#xD;
	18. Salehi S, Boddohi S. New formulation and approach for mucoadhesive buccal film of rizatriptan benzoate. Progress in biomaterials. 2017; 6: 175-187.&#xD;
	19. De Ascentiis A, Degrazia JL, Bowman CN, Colombo P, Peppas NA. Mucoadhesion of poly (2-hydroxyethyl methacrylate) is improved when linear poly (ethylene oxide) chains are added to the polymer network. Journal of controlled release (JCR). 1995;&#xA0;33 (1): 197-201.&#xD;
	20. Brako F, Raimi-Abraham B, Mahalingam S, Craig DQ, Edirisinghe M. Making nanofibres of mucoadhesive polymer blends for vaginal therapies. European Polymer Journal. 2015; 70: 186- 196.&#xD;
	21. Mahalingam R, Jasti B, Birudaraj R, Stefanidis D, Killion R. Alfredson T. et al. Evaluation of polyethylene oxide compacts as gastroretentive delivery systems. AAPS PharmSciTech. 2009; 10: 98-103.&#xD;
	22. Raut DS, Rohera BD. Formulation, in vitro evaluation and study of variables on tri-layered gastro-retentive delivery system of diltiazem HCl. Drug development and industrial pharmacy. 2014; 40 (3): 380-389.&#xD;
	23. Sharma OP, Shah MV, Parikh DC, Mehta TA. Formulation optimization of gastroretentive drug delivery system for allopurinol using experimental design. Expert Opinion on Drug Delivery. 2015; 12 (4): 513-524.&#xD;
	24. Liu Q, Fassihi R. Zero-order delivery of a highly soluble, low dose drug alfuzosin hydrochloride via gastro-retentive system. Inter J Pharm. 2008; 348 (1-2): 27-34.&#xD;
	25. Senjoti FG, Jaffri JM, Mandal UK. In Fabrication and optimization of gastro retentive drug delivery system with HPMC and polyethylene oxide (PEO) matrix, International Conference on Pharmaceutical Sciences and Biomedical and Chemical Engineering. Kuantan, Malaysia: Kulliyyah of Pharmacy International Islamic University Malaysia (IIUM). 2014; pp 113-7.&#xD;
	26. Cantin O, Siepmann F, Danede F, Willart J, Karrout Y, Siepmann J. PEO hot melt extrudates for controlled drug delivery: Importance of the molecular weight. Journal of Drug Delivery Science and Technology. 2016; 36:; 130-140.&#xD;
	27. Crowley MM, Zhang F, Koleng JJ, McGinity JW. Stability of polyethylene oxide in matrix tablets prepared by hot-melt extrusion. Biomaterials. 2002; 23 (21): 4241-4248.&#xD;
	28. Cantin O, Siepmann F, Willart JF, Danede F, Siepmann J, Karrout Y. PEO hot melt extrudates for controlled drug delivery: Importance of the type of drug and loading. J Drug Deliv SciTechnol. 2021; 61: 102-238.&#xD;
	29. Crowley M M, Fredersdorf A, Schroeder B, Kucera S, Prodduturi S, Repka M A, et al. The influence of guaifenesin and ketoprofen on the properties of hot-melt extruded polyethylene oxide films. Eur J Pharm Sci. 2004; 22 (5): 409-418.&#xD;
	30. Li L, AbuBaker O, Shao Z J. Characterization of poly (ethylene oxide) as a drug carrier in hot-melt extrusion. Drug development and industrial pharmacy. 2006;32 (8): 991-1002.&#xD;
&#xD;
&#xD;
&#xD;
	&#xA0;&#xD;
&#xD;
</References></Article></ArticleSet></xml>
