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Preparation of Starch/Gelatin Blend Microparticles by a Water-in-Oil Emulsion Method for Controlled Release Drug Delivery.

International journal of biomaterials

Phromsopha T, Baimark Y.
PMID: 24868207
Int J Biomater. 2014;2014:829490. doi: 10.1155/2014/829490. Epub 2014 Apr 29.

Information on the preparation and properties of starch/gelatin blend microparticles with and without crosslinking for drug delivery is presented. The blend microparticles were prepared by the water-in-oil emulsion solvent diffusion method. Glutaraldehyde and methylene blue were used as the...

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Phromsopha T, Baimark Y. Preparation of Starch/Gelatin Blend Microparticles by a Water-in-Oil Emulsion Method for Controlled Release Drug Delivery. Int J Biomater. 2014;2014:829490doi: 10.1155/2014/829490.
Phromsopha, T., & Baimark, Y. (2014). Preparation of Starch/Gelatin Blend Microparticles by a Water-in-Oil Emulsion Method for Controlled Release Drug Delivery. International journal of biomaterials, 2014829490. https://doi.org/10.1155/2014/829490
Phromsopha, Theeraphol, and Baimark, Yodthong. "Preparation of Starch/Gelatin Blend Microparticles by a Water-in-Oil Emulsion Method for Controlled Release Drug Delivery." International journal of biomaterials vol. 2014 (2014): 829490. doi: https://doi.org/10.1155/2014/829490
Phromsopha T, Baimark Y. Preparation of Starch/Gelatin Blend Microparticles by a Water-in-Oil Emulsion Method for Controlled Release Drug Delivery. Int J Biomater. 2014;2014:829490. doi: 10.1155/2014/829490. Epub 2014 Apr 29. PMID: 24868207; PMCID: PMC4020388.
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Strikingly simple direct alpha-allylation of aldehydes with allyl alcohols: remarkable advance in the Tsuji-Trost reaction.

Journal of the American Chemical Society

Kimura M, Horino Y, Mukai R, Tanaka S, Tamaru Y.
PMID: 11603997
J Am Chem Soc. 2001 Oct 24;123(42):10401-2. doi: 10.1021/ja011656a.

No abstract available.

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Kimura M, Horino Y, Mukai R, et al. Strikingly simple direct alpha-allylation of aldehydes with allyl alcohols: remarkable advance in the Tsuji-Trost reaction. J Am Chem Soc. 2001;123(42):10401-2doi: 10.1021/ja011656a.
Kimura, M., Horino, Y., Mukai, R., Tanaka, S., & Tamaru, Y. (2001). Strikingly simple direct alpha-allylation of aldehydes with allyl alcohols: remarkable advance in the Tsuji-Trost reaction. Journal of the American Chemical Society, 123(42), 10401-2. https://doi.org/10.1021/ja011656a
Kimura, M, et al. "Strikingly simple direct alpha-allylation of aldehydes with allyl alcohols: remarkable advance in the Tsuji-Trost reaction." Journal of the American Chemical Society vol. 123,42 (2001): 10401-2. doi: https://doi.org/10.1021/ja011656a
Kimura M, Horino Y, Mukai R, Tanaka S, Tamaru Y. Strikingly simple direct alpha-allylation of aldehydes with allyl alcohols: remarkable advance in the Tsuji-Trost reaction. J Am Chem Soc. 2001 Oct 24;123(42):10401-2. doi: 10.1021/ja011656a. PMID: 11603997.
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Remarkably high 1,5-diastereoselectivity in a nickel-catalyzed conjugate addition of Me(2)Zn and carbonyl compounds to 1,omega-dienynes with through-space coupling.

Angewandte Chemie (International ed. in English)

Ezoe A, Kimura M, Inoue T, Mori M, Tamaru Y.
PMID: 12203485
Angew Chem Int Ed Engl. 2002 Aug 02;41(15):2784-6. doi: 10.1002/1521-3773(20020802)41:15<2784::AID-ANIE2784>3.0.CO;2-A.

No abstract available.

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Ezoe A, Kimura M, Inoue T, et al. Remarkably high 1,5-diastereoselectivity in a nickel-catalyzed conjugate addition of Me(2)Zn and carbonyl compounds to 1,omega-dienynes with through-space coupling. Angew Chem Int Ed Engl. 2002;41(15):2784-6doi: 10.1002/1521-3773(20020802)41:15<2784::AID-ANIE2784>3.0.CO;2-A.
Ezoe, A., Kimura, M., Inoue, T., Mori, M., & Tamaru, Y. (2002). Remarkably high 1,5-diastereoselectivity in a nickel-catalyzed conjugate addition of Me(2)Zn and carbonyl compounds to 1,omega-dienynes with through-space coupling. Angewandte Chemie (International ed. in English), 41(15), 2784-6. https://doi.org/10.1002/1521-3773(20020802)41:15<2784::AID-ANIE2784>3.0.CO;2-A
Ezoe, Akihiro, et al. "Remarkably high 1,5-diastereoselectivity in a nickel-catalyzed conjugate addition of Me(2)Zn and carbonyl compounds to 1,omega-dienynes with through-space coupling." Angewandte Chemie (International ed. in English) vol. 41,15 (2002): 2784-6. doi: https://doi.org/10.1002/1521-3773(20020802)41:15<2784::AID-ANIE2784>3.0.CO;2-A
Ezoe A, Kimura M, Inoue T, Mori M, Tamaru Y. Remarkably high 1,5-diastereoselectivity in a nickel-catalyzed conjugate addition of Me(2)Zn and carbonyl compounds to 1,omega-dienynes with through-space coupling. Angew Chem Int Ed Engl. 2002 Aug 02;41(15):2784-6. doi: 10.1002/1521-3773(20020802)41:15<2784::AID-ANIE2784>3.0.CO;2-A. PMID: 12203485.
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Nickel-catalyzed intramolecular homoallylation of omega-dienyl aldehyde.

Organic letters

Shibata K, Kimura M, Shimizu M, Tamaru Y.
PMID: 11440574
Org Lett. 2001 Jul 12;3(14):2181-3. doi: 10.1021/ol0100879.

[reaction: see text] In the presence of a catalytic amount of Ni(acac)(2), Et(3)B and Et(2)Zn nicely promote a reductive homoallylic cyclization of omega-dienyl aldehydes and provide 2-allylcyclopentanols and -cyclohexanols with high stereoselectivity in excellent yield. The reaction requires only...

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Shibata K, Kimura M, Shimizu M, et al. Nickel-catalyzed intramolecular homoallylation of omega-dienyl aldehyde. Org Lett. 2001;3(14):2181-3doi: 10.1021/ol0100879.
Shibata, K., Kimura, M., Shimizu, M., & Tamaru, Y. (2001). Nickel-catalyzed intramolecular homoallylation of omega-dienyl aldehyde. Organic letters, 3(14), 2181-3. https://doi.org/10.1021/ol0100879
Shibata, K, et al. "Nickel-catalyzed intramolecular homoallylation of omega-dienyl aldehyde." Organic letters vol. 3,14 (2001): 2181-3. doi: https://doi.org/10.1021/ol0100879
Shibata K, Kimura M, Shimizu M, Tamaru Y. Nickel-catalyzed intramolecular homoallylation of omega-dienyl aldehyde. Org Lett. 2001 Jul 12;3(14):2181-3. doi: 10.1021/ol0100879. PMID: 11440574.
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Pd-catalyzed nucleophilic alkylation of aliphatic aldehydes with allyl alcohols: allyl, 2-tetrahydrofuryl, and 2-tetrahydropyranyl ethers as useful C3, C4, and C5 sources.

Angewandte Chemie (International ed. in English)

Kimura M, Shimizu M, Shibata K, Tazoe M, Tamaru Y.
PMID: 12888967
Angew Chem Int Ed Engl. 2003 Jul 28;42(29):3392-5. doi: 10.1002/anie.200351182.

No abstract available.

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Kimura M, Shimizu M, Shibata K, et al. Pd-catalyzed nucleophilic alkylation of aliphatic aldehydes with allyl alcohols: allyl, 2-tetrahydrofuryl, and 2-tetrahydropyranyl ethers as useful C3, C4, and C5 sources. Angew Chem Int Ed Engl. 2003;42(29):3392-5doi: 10.1002/anie.200351182.
Kimura, M., Shimizu, M., Shibata, K., Tazoe, M., & Tamaru, Y. (2003). Pd-catalyzed nucleophilic alkylation of aliphatic aldehydes with allyl alcohols: allyl, 2-tetrahydrofuryl, and 2-tetrahydropyranyl ethers as useful C3, C4, and C5 sources. Angewandte Chemie (International ed. in English), 42(29), 3392-5. https://doi.org/10.1002/anie.200351182
Kimura, Masanari, et al. "Pd-catalyzed nucleophilic alkylation of aliphatic aldehydes with allyl alcohols: allyl, 2-tetrahydrofuryl, and 2-tetrahydropyranyl ethers as useful C3, C4, and C5 sources." Angewandte Chemie (International ed. in English) vol. 42,29 (2003): 3392-5. doi: https://doi.org/10.1002/anie.200351182
Kimura M, Shimizu M, Shibata K, Tazoe M, Tamaru Y. Pd-catalyzed nucleophilic alkylation of aliphatic aldehydes with allyl alcohols: allyl, 2-tetrahydrofuryl, and 2-tetrahydropyranyl ethers as useful C3, C4, and C5 sources. Angew Chem Int Ed Engl. 2003 Jul 28;42(29):3392-5. doi: 10.1002/anie.200351182. PMID: 12888967.
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Nickel(0)-Catalyzed Three-Component Connection Reaction of Dimethylzinc, 1,3-Dienes, and Carbonyl Compounds.

Angewandte Chemie (International ed. in English)

Kimura M, Matsuo S, Shibata K, Tamaru Y.
PMID: 10602204
Angew Chem Int Ed Engl. 1999 Nov 15;38(22):3386-3388. doi: 10.1002/(sici)1521-3773(19991115)38:22<3386::aid-anie3386>3.0.co;2-w.

Linear 1:1:1 coupling of dimethylzinc, 1,3-dienes, and carbonyl compounds in this order is facilitated by catalytic amounts of [Ni(acac)(2)] to give (E)-3-hexen-1-ols in good yields under mild conditions [Eq. (a)]. Increasing steric hindrance at the carbonyl group favors formation...

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Kimura M, Matsuo S, Shibata K, et al. Nickel(0)-Catalyzed Three-Component Connection Reaction of Dimethylzinc, 1,3-Dienes, and Carbonyl Compounds. Angew Chem Int Ed Engl. 1999;38(22):3386-3388doi: 10.1002/(sici)1521-3773(19991115)38:22<3386::aid-anie3386>3.0.co;2-w.
Kimura, M., Matsuo, S., Shibata, K., & Tamaru, Y. (1999). Nickel(0)-Catalyzed Three-Component Connection Reaction of Dimethylzinc, 1,3-Dienes, and Carbonyl Compounds. Angewandte Chemie (International ed. in English), 38(22), 3386-3388. https://doi.org/10.1002/(sici)1521-3773(19991115)38:22<3386::aid-anie3386>3.0.co;2-w
Kimura, et al. "Nickel(0)-Catalyzed Three-Component Connection Reaction of Dimethylzinc, 1,3-Dienes, and Carbonyl Compounds." Angewandte Chemie (International ed. in English) vol. 38,22 (1999): 3386-3388. doi: https://doi.org/10.1002/(sici)1521-3773(19991115)38:22<3386::aid-anie3386>3.0.co;2-w
Kimura M, Matsuo S, Shibata K, Tamaru Y. Nickel(0)-Catalyzed Three-Component Connection Reaction of Dimethylzinc, 1,3-Dienes, and Carbonyl Compounds. Angew Chem Int Ed Engl. 1999 Nov 15;38(22):3386-3388. doi: 10.1002/(sici)1521-3773(19991115)38:22<3386::aid-anie3386>3.0.co;2-w. PMID: 10602204.
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Highly stereo- and regioselective ni-catalyzed homoallylation of aldimines with conjugated dienes promoted by diethylzinc.

Journal of the American Chemical Society

Kimura M, Miyachi A, Kojima K, Tanaka S, Tamaru Y.
PMID: 15521748
J Am Chem Soc. 2004 Nov 10;126(44):14360-1. doi: 10.1021/ja0450354.

Under the nickel catalysis, in one pot, diethylzinc serves as a reducing agent to connect the three components of 1,3-dienes, alkyl or aryl aldehydes, and anilines to furnish 3-substituted 3,5-syn-5-(arylamino)pent-1-enes 1, the homoallylation products of aldimines with dienes, in...

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Kimura M, Miyachi A, Kojima K, et al. Highly stereo- and regioselective ni-catalyzed homoallylation of aldimines with conjugated dienes promoted by diethylzinc. J Am Chem Soc. 2004;126(44):14360-1doi: 10.1021/ja0450354.
Kimura, M., Miyachi, A., Kojima, K., Tanaka, S., & Tamaru, Y. (2004). Highly stereo- and regioselective ni-catalyzed homoallylation of aldimines with conjugated dienes promoted by diethylzinc. Journal of the American Chemical Society, 126(44), 14360-1. https://doi.org/10.1021/ja0450354
Kimura, Masanari, et al. "Highly stereo- and regioselective ni-catalyzed homoallylation of aldimines with conjugated dienes promoted by diethylzinc." Journal of the American Chemical Society vol. 126,44 (2004): 14360-1. doi: https://doi.org/10.1021/ja0450354
Kimura M, Miyachi A, Kojima K, Tanaka S, Tamaru Y. Highly stereo- and regioselective ni-catalyzed homoallylation of aldimines with conjugated dienes promoted by diethylzinc. J Am Chem Soc. 2004 Nov 10;126(44):14360-1. doi: 10.1021/ja0450354. PMID: 15521748.
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Revision of the predictive method improves precision in the prediction of stroke outcomes for patients admitted to rehabilitation hospitals.

Journal of physical therapy science

Matsugi A, Tani K, Mitani Y, Oku K, Tamaru Y, Nagano K.
PMID: 25276029
J Phys Ther Sci. 2014 Sep;26(9):1429-31. doi: 10.1589/jpts.26.1429. Epub 2014 Sep 17.

[Purpose] The purpose of this study was to confirm the accuracy of a revised method for predicting the Functional Independence Measure (FIM) at discharge when stroke patients are first admitted to a rehabilitation hospital. [Subjects and Methods] The predictive...

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Matsugi A, Tani K, Mitani Y, et al. Revision of the predictive method improves precision in the prediction of stroke outcomes for patients admitted to rehabilitation hospitals. J Phys Ther Sci. 2014;26(9):1429-31doi: 10.1589/jpts.26.1429.
Matsugi, A., Tani, K., Mitani, Y., Oku, K., Tamaru, Y., & Nagano, K. (2014). Revision of the predictive method improves precision in the prediction of stroke outcomes for patients admitted to rehabilitation hospitals. Journal of physical therapy science, 26(9), 1429-31. https://doi.org/10.1589/jpts.26.1429
Matsugi, Akiyoshi, et al. "Revision of the predictive method improves precision in the prediction of stroke outcomes for patients admitted to rehabilitation hospitals." Journal of physical therapy science vol. 26,9 (2014): 1429-31. doi: https://doi.org/10.1589/jpts.26.1429
Matsugi A, Tani K, Mitani Y, Oku K, Tamaru Y, Nagano K. Revision of the predictive method improves precision in the prediction of stroke outcomes for patients admitted to rehabilitation hospitals. J Phys Ther Sci. 2014 Sep;26(9):1429-31. doi: 10.1589/jpts.26.1429. Epub 2014 Sep 17. PMID: 25276029; PMCID: PMC4175250.
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Toughening of Poly(L-lactide) with Blends of Poly(.

International journal of biomaterials

Srisuwan Y, Baimark Y, Suttiruengwong S.
PMID: 30275834
Int J Biomater. 2018 Sep 12;2018:1294397. doi: 10.1155/2018/1294397. eCollection 2018.

A poly(

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Srisuwan Y, Baimark Y, Suttiruengwong S. Toughening of Poly(L-lactide) with Blends of Poly(. Int J Biomater. 2018;2018:1294397doi: 10.1155/2018/1294397.
Srisuwan, Y., Baimark, Y., & Suttiruengwong, S. (2018). Toughening of Poly(L-lactide) with Blends of Poly(. International journal of biomaterials, 20181294397. https://doi.org/10.1155/2018/1294397
Srisuwan, Yaowalak, et al. "Toughening of Poly(L-lactide) with Blends of Poly(." International journal of biomaterials vol. 2018 (2018): 1294397. doi: https://doi.org/10.1155/2018/1294397
Srisuwan Y, Baimark Y, Suttiruengwong S. Toughening of Poly(L-lactide) with Blends of Poly(. Int J Biomater. 2018 Sep 12;2018:1294397. doi: 10.1155/2018/1294397. eCollection 2018. PMID: 30275834; PMCID: PMC6157148.
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Use of anticoagulants increases risk of bleeding after colorectal endoscopic submucosal dissection.

Endoscopy international open

Yamashita K, Oka S, Tanaka S, Boda K, Hirano D, Sumimoto K, Mizumoto T, Ninomiya Y, Tamaru Y, Shigita K, Hayashi N, Sanomura Y, Chayama K.
PMID: 29978006
Endosc Int Open. 2018 Jul;6(7):E857-E864. doi: 10.1055/a-0593-5788. Epub 2018 Jul 04.

BACKGROUND AND STUDY AIMS : Japanese guidelines for gastroenterological endoscopy have recommended temporary withdrawal of anticoagulants (warfarin, direct oral anticoagulants [DOAC], or heparin) to prevent hemorrhagic complications during endoscopic submucosal dissection (ESD) for colorectal neoplasias (CRNs). However, serious thrombosis...

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Yamashita K, Oka S, Tanaka S, et al. Use of anticoagulants increases risk of bleeding after colorectal endoscopic submucosal dissection. Endosc Int Open. 2018;6(7):E857-E864doi: 10.1055/a-0593-5788.
Yamashita, K., Oka, S., Tanaka, S., Boda, K., Hirano, D., Sumimoto, K., Mizumoto, T., Ninomiya, Y., Tamaru, Y., Shigita, K., Hayashi, N., Sanomura, Y., & Chayama, K. (2018). Use of anticoagulants increases risk of bleeding after colorectal endoscopic submucosal dissection. Endoscopy international open, 6(7), E857-E864. https://doi.org/10.1055/a-0593-5788
Yamashita, Ken, et al. "Use of anticoagulants increases risk of bleeding after colorectal endoscopic submucosal dissection." Endoscopy international open vol. 6,7 (2018): E857-E864. doi: https://doi.org/10.1055/a-0593-5788
Yamashita K, Oka S, Tanaka S, Boda K, Hirano D, Sumimoto K, Mizumoto T, Ninomiya Y, Tamaru Y, Shigita K, Hayashi N, Sanomura Y, Chayama K. Use of anticoagulants increases risk of bleeding after colorectal endoscopic submucosal dissection. Endosc Int Open. 2018 Jul;6(7):E857-E864. doi: 10.1055/a-0593-5788. Epub 2018 Jul 04. PMID: 29978006; PMCID: PMC6031438.
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Identification of Major Compounds and α-Amylase and α-Glucosidase Inhibitory Activity of Rhizome of Musa balbisiana Colla: An In-vitro and insilico Study.

Combinatorial chemistry & high throughput screening

Swargiary A, Daimari M.
PMID: 33234097
Comb Chem High Throughput Screen. 2020 Nov 24; doi: 10.2174/1386207323666201124144332. Epub 2020 Nov 24.

BACKGROUND: α-Amylase and α-glucosidase inhibitors are widely used to suppress postprandial glycemia in the treatment of type 2 diabetes.OBJECTIVES: To evaluate the metallic content, major phytoconstituents, and α-amylase and α-glucosidase inhibitory activity of Musa balbisiana rhizome using in-vitro and...

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Swargiary A, Daimari M. Identification of Major Compounds and α-Amylase and α-Glucosidase Inhibitory Activity of Rhizome of Musa balbisiana Colla: An In-vitro and insilico Study. Comb Chem High Throughput Screen. 2020;doi: 10.2174/1386207323666201124144332.
Swargiary, A., & Daimari, M. (2020). Identification of Major Compounds and α-Amylase and α-Glucosidase Inhibitory Activity of Rhizome of Musa balbisiana Colla: An In-vitro and insilico Study. Combinatorial chemistry & high throughput screening, . https://doi.org/10.2174/1386207323666201124144332
Swargiary, Ananta, and Daimari, Manita. "Identification of Major Compounds and α-Amylase and α-Glucosidase Inhibitory Activity of Rhizome of Musa balbisiana Colla: An In-vitro and insilico Study." Combinatorial chemistry & high throughput screening vol. (2020). doi: https://doi.org/10.2174/1386207323666201124144332
Swargiary A, Daimari M. Identification of Major Compounds and α-Amylase and α-Glucosidase Inhibitory Activity of Rhizome of Musa balbisiana Colla: An In-vitro and insilico Study. Comb Chem High Throughput Screen. 2020 Nov 24; doi: 10.2174/1386207323666201124144332. Epub 2020 Nov 24. PMID: 33234097.
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Current clinical developments in curcumin-based therapeutics for cancer and chronic diseases.

Phytotherapy research : PTR

Kumar A, Harsha C, Parama D, Girisa S, Daimary UD, Mao X, Kunnumakkara AB.
PMID: 34498308
Phytother Res. 2021 Sep 08; doi: 10.1002/ptr.7264. Epub 2021 Sep 08.

The last decade has seen an unprecedented rise in the prevalence of chronic diseases worldwide. Different mono-targeted approaches have been devised to treat these multigenic diseases, still most of them suffer from limited success due to the off-target debilitating...

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Kumar A, Harsha C, Parama D, et al. Current clinical developments in curcumin-based therapeutics for cancer and chronic diseases. Phytother Res. 2021;doi: 10.1002/ptr.7264.
Kumar, A., Harsha, C., Parama, D., Girisa, S., Daimary, U. D., Mao, X., & Kunnumakkara, A. B. (2021). Current clinical developments in curcumin-based therapeutics for cancer and chronic diseases. Phytotherapy research : PTR, . https://doi.org/10.1002/ptr.7264
Kumar, Aviral, et al. "Current clinical developments in curcumin-based therapeutics for cancer and chronic diseases." Phytotherapy research : PTR vol. (2021). doi: https://doi.org/10.1002/ptr.7264
Kumar A, Harsha C, Parama D, Girisa S, Daimary UD, Mao X, Kunnumakkara AB. Current clinical developments in curcumin-based therapeutics for cancer and chronic diseases. Phytother Res. 2021 Sep 08; doi: 10.1002/ptr.7264. Epub 2021 Sep 08. PMID: 34498308.
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