ORIGINAL_ARTICLE
Nano CeO2 as a new green and recyclable catalyst for the synthesis of 2-aryl Benzoxazole
2-Aryl benzoxazole derivatives have been reported to have a wide range of biological and pharmacological activities. Some of these derivatives have anticoagulant, antispasmodic, diuretic, anti-cancer and anti-anaphylactin properties. In this research, a simple method for the synthesis of high-efficiency 2-aryl benzoxazole through the reaction of aminophenols and aldehyde derivatives under solvent-free conditions in the presence of a catalytic amount of nano-CeO2 is presented. The results revealed that this synthetic reaction is very simple and benzoxazole derivatives produced with good yields compared to other studies. Mild conditions, high speed and short reaction time, simplicity of product separation process, high efficiency and purity of synthesized derivatives are the advantages of the proposed method. As shown in Table 5, the highest efficiency (95%) in a short time (15 min) was obtained in this study, which is very important compared to other previous methods presented.
https://www.ajnanomat.com/article_132310_42863a385b14df1f3311689c8432b4d1.pdf
2021-10-01
255
262
10.26655/AJNANOMAT.2021.4.1
Nano
CeO2 O
aminophenols Aldehydes 2
Arylbenzoxazole
Bita
Baghernejad
bitabaghernejad@yahoo.com
1
Department of Chemistry, Payame Noor University, PO BOX 19395-4697 Tehran, Iran
LEAD_AUTHOR
Reyhaneh
Samaie
2
Department of Chemistry, Payame Noor University, PO BOX 19395-4697 Tehran, Iran
LEAD_AUTHOR
[1]. Chaney M.O., Demarco P.V., Jones N.D., Occolowitz J.L. J. Am. Chem. Soc.,1974, 96:1932
1
[2]. Ueki M., Ueno K., Miyadoh S., Abe K., Shibata K., Taniguchi M., Oi S. J. Antibiot.,1993, 46:1089
2
[3]. Sato Y., Yamada M., Yoshida S., Soneda T., Ishikawa M., Nizato T., Suzuki K., Konno F. J. Med. Chem.,1998, 41:3015
3
[4]. Chen P., Cheng P.T.W., Alam M., Beyer B.D., Bisacchi G.S., Dejneka T., Evans A.J., Greytok J.A., Hermsmeier M.A., Humphreys W.G., Jacobs G.A., Kocy O., Lin P.F., Lis K.A., Marella M.A., Ryono D.E., Sheaffer A.K., Spergel S.H., Sun C.q., Tino J.A., Vite G., Colonno R.J., Zahler R., Barrish J.C. J. Med. Chem.,1996, 39:1991
4
[5]. Paramshivappa R., Kumar P.P., Subba Rao P.V., Srinivase Rao A. Bioorg. Med. Chem. Lett., 2003, 13:657
5
[6]. Costanzo M.J., Maryanoff B.E., Hecker L.R., Schott M.R., Yabut S.C., Zhang H.C., Andrade-Gordon P., Kauffman J.A., Lewis J.M., Krishnan R., Tulinski A. J.Med. Chem., 1996, 39:3039
6
[7]. Meyer M.D., Hancock A.A., Tietje K., Sippy K.B., Prasad R., Stout D.M., Arendsen D.L., Donner B.G., Carroll W.A. J. Med. Chem., 1997, 40:1049
7
[8]. Ogilvie W., Bailey M., Poupart M.A., Abraham A., Bhavsar A., Bonneau P., Bordeleau J., Bousquet Y., Chabot C., Duceppe J.S., Fazal G., Goulet S., Grand-Maıˆtre C., Guse I., Halmos T., Lavalle´e P., Leach M., Malefant E., O’Meara J., Plante R., Plouffe C., Poirier M., Soucy F., Yoakim C., De´ziel R. J. Med. Chem.,1997, 40:4113
8
[9]. Temiz O., Rren I., Sener E., Yalcin I., Ucarturk N. Farmaco,1998, 53:337
9
[10]. Sato S., Kajiura T., Noguchi M., Takehana K., Kobayashi T., Tsuji T. J. Antibiot., 2001, 54:102
10
[11]. Ivanov S.K.N., Yuritsyn V.S. Chem. Abstr., 1971, 74:124487m
11
[12]. Monsanto C. Chem. Abstr., 1968, 68:96660t
12
[13]. Sato S., Kajiura T., Noguchi M., Takehana K., Kobayashi T., Tsuji T. J. Antibiot., 2001, 54:102
13
[14]. Terashima M., Ishii M. Synthesis,1982, 1484
14
[15]. Varma R.S., Saini R.K., Prakash O. Tetrahedron Lett., 1997, 38:2621
15
[16]. Varma R.S., Kumar D. J. Heterocyclic Chem., 1998, 35:1539
16
[17]. Melchionna M., Fornasiero P. Material. Today., 2014, 17:349
17
[18]. Muthuchudarkodi R.R., Kalaiarasi S. J. Scienc. Research., 2016, 5:543
18
[19]. Varma R.S., Saini R.K., Parkash O. Tetrahedron. Lett., 1997, 38:2621
19
[20]. Liu Y.K., Mao D.J., Lou Sh.J., Qian J.Q., Xu Zh.Y. J. Zhejiang. Univ. Sci. B., 2009, 10:472
20
[21]. Kawashita K., Nakamichi N, Kawabata H., Hayashi M. Org. Lett., 2003, 5:2317
21
[22]. Naeimi H., Rouzegar Z., Rahmantinejad S. Synth. Commun., 2017, 47:2087
22
[23]. Patil M.R., Bhanushali J.T., Nagaraja B.M., Keri R.S., Compt. Rendus. Chimie., 2018, 21:399
23
ORIGINAL_ARTICLE
Green synthesis of CoFe2O4 ferrofluid: Investigation of structural, magnetic and rheological behaviour
In this work, we report the green synthesis of cobalt ferrite (CoFe2O4) nanoparticles Ferrofluid by a modified co-precipitation method using Glycyrrhiza glabra (Licorice) roots as a surfactant, which is eco-friendly, non-toxic, and inexpensive. X-Ray diffraction (XRD) analysis confirmed the purity of the spinel CoFe2O4 structure. The average crystallite size, strain and lattice constant were 5 nm, 0.01, and 8.39 Ao, respectively. Fourier transform infrared spectrum (FTIR) results demonstrated an absorption band at a wavenumber of 574 cm-1, indicating the presence of cobalt ferrite nanoparticles. transmission electron microscopy (TEM) images showed that the sample contains well-dispersed and spherical nanoparticles with an average particle size of 12.6 nm. The magnetic properties of the fluid are confirmed from the (M-H) hysteresis curve. The hysteresis curve revealed the ferromagnetic nature of the particles, and the saturation magnetization (MS) is 56.6 emu/g. The rheological properties were studied with a variable magnetic field rheometer. The results showed that the rheological measurements comply with the structural and magnetic properties of the CFO FF by a green modified co-precipitation synthesis G. glabra, which can be used for various medical applications.
https://www.ajnanomat.com/article_134104_d31c11ff3ce3dc02a918508311a05c6d.pdf
2021-10-01
263
273
10.26655/AJNANOMAT.2021.4.2
Green synthesis
Cobalt ferrite
ferrofluid
Rheology
Magnetization
Meet A.
Moradiya
meetmoradiya2812@gmail.com
1
School of Nanotechnology, Rajiv Gandhi Proudyogiki Vishwavidyalaya, Bhopal, Madhya Pradesh, India
LEAD_AUTHOR
Pradeep
Khiriya
pradeep.khiriya@gmaiil.com
2
School of Nanotechnology, Rajiv Gandhi Proudyogiki Vishwavidyalaya, Bhopal, Madhya Pradesh, India
AUTHOR
Purnima Swarup
Khare
purnimask19@gmail.com
3
School of Nanotechnology, Rajiv Gandhi Proudyogiki Vishwavidyalaya, Bhopal, Madhya Pradesh, India
AUTHOR
[1]. Pillai V., Shah D.O. J. Magn. Magn. Mater., 1996, 163:243
1
[2]. Zain N.M., Shafi A.A. J. Adv. Res. Mater. Sci., 2016, 26:1
2
[3]. Fried T., Shemer G., Markovich G. Adv. Mater., 2001, 13:1158
3
[4]. Sheikholeslami M., Shehzad S.A. Int. J. Heat Mass Transf., 2017, 109:82
4
[5]. Zakinyan A.R., Dikansky Y.I. J. Magn. Magn. Mater., 2017, 431:103
5
[6]. Yang C., Yu M., Zhao S., Tian Y., Bian X. Nanoscale Res. Lett., 2018, 13:1
6
[7]. Özbey A., Karimzadehkhouei M., Yalçın S.E., Gozuacik D., Koşar A. Microfluid.Nanofluidics., 2015, 18:447
7
[8]. Pala J., Mehta H., Mandaliya R., Moradiya M., Savaliya C.R., Markna J.H. MOJ Biol. Med., 2017, 2:174
8
[9]. Moradiya M.A., Ladani A., Ladani J., Raiyani Markna J.H. J ChemSci Eng., 2017, 2:58
9
[10]. Nakatsuka K., Jeyadevan B., Neveu S., Koganezawa H. J. Magn. Magn. Mater., 2002, 252:360
10
[11]. Song J., Wang L., Xu N., Zhang Q. J. Rare Earths., 2010, 28:451
11
[12]. Homa D., Pickrell G. 2014, 14:3891
12
[13]. Naseri M.G., Saion E.B., Ahangar H.A., Shaari A.H., Hashim M. Journal of Nanomaterials, 2010, 2010:8 paages
13
[14]. Anastas P.T., Warner J.C. Oxford University Press, 1998
14
[15]. Ezzatzadeh E. De Gruyter, 2018, 73(3-4)b:179
15
[16]. Ezzatzadeh E., Sofla S.F.I., Pourghasem E., Rustaiyan A., Zarezadeh Z. J. Essent. Oil-Bear. Plants., 2014, 17:415
16
[17]. Fardood S.T., Moradnia F., Ghalaichi A.H., Daneshpajooh Sh., Heidari M. NanochemRes., 2020, 5:69
17
[18]. Bhanvase B., Pawade V., Dhoble S.J., S. Sonawane S., Muthupandian A. Elsevier, 2018
18
[19]. Fardood S.T., Ramazani A., Golfar Z., Joo S.W. J. Appl. Chem. Res., 2017, 11:19
19
[20]. Fardood S.T., Moradnia F., Moradi S., Forootan R., Yekke Z.F., Heidari M. Nanochem Res., 2019, 4:140
20
[21]. Fardood S.T., Moradnia F., Mostafaei M., Afshari Z., Faramarzi V., Ganjkhanlu S. Nanochem Res., 2019, 4:86
21
[22]. Amini I., Azizkhani V., Ezzatzadeh E., Pal K., Rezayati S., Fekri M.H., Shirkhani P. Asian J. Green Chem., 2020, 4:51
22
[23]. Ezzatzadeh E., Hossaini Z. Nat. Prod. Res., 2020, 34:923
23
[24]. Ezzatzadeh E., Hossaini Z., Rostamian R., Vaseghi S., Mousavi S.F. J. Heterocyclic Chem., 2017
24
[25]. Atrak K., Ramazani A., Fardood S.T. Environ. Technol., 2020, 41:2760
25
[26]. Moradnia F., Fardood S.T., Ramazani A., Osali S., Abdolmaleki I. Micro Nano Lett., 2020, 15:674
26
[27]. Moradniaa F., Fardood S.T., Ramazani A., Minc B., WooJood S., Varma R.S. J. Cleaner Prod., 2021, 288:125632
27
[28]. Ahankara H., Fardood S.T., Ramazanib A. Iran. J. Catal., 2020, 10:195
28
[29]. Ezzatzadeh E., Hossaini Z., Moradi A.V., Salimifard M., Sharif Abad S.A. Can. J. Chem., 2019, 97:270
29
[30]. Amini I., Azizkhani V., Ezzatzadeh Z., Pal K., Rezayati S., Fekri M.H., Shirkhani P. Asian J. Green Chem., 2020, 4:51
30
[31]. Mansour S.S., Ezzatzadeh E., Safarkar R. Asian J. Green Chem., 2019, 3:353
31
[32]. Jivani A., Moradiya M.A. J. Sci. Technol., 2020, 5:213
32
[33]. Moradiya M.A., Dangodara A., Pala J., Savaliya C.R., Dhruv D., Rathod V.R., Joshi A.D., Shah N.A., Pandya D., Markna J.H. Sep. Sci. Technol., 2019, 54:207
33
[34]. Shaikh R., Syed I.Z., Bhende P. Asian J. Green Chem., 2019, 3:70
34
[35]. Manikandan M., Durka S., Antony A. J. Inorg. Organomet. Polym., 2015, 25:1019
35
[36]. Gingaşu D., Mîndru I., preda S., calderon-moreno J.M., culiţǎ L. patrona D.C., diamandescub L. Rev. Roum. Chim., 2017, 62:645
36
[37]. Kombaiah K., Vijaya J.J., Kennedy L.J., Bououdina M., Ramalingam R.J., Al-Lohedan H.A. Mater. Chem. Phys., 2018, 204:410
37
[38]. Anburaj R., Jothiprakasam V., Nadu T. International Journal of Pharmaceutical Sciences Review and Research, 2018, 51:137
38
[39]. Shahmiria N., Manteghi F., Sohrabia B., Golafshanb S., The 18th International Electronic Conference on Synthetic Organic Chemistry, 2013, 31:924
39
[40]. Al-snafi A.E. IOSR J. Pharm., 2018, 8:1
40
[41]. Kalsi S., Verma S.K., Kaur A., Singh N. Int. J. Pharm. Drug Anal., 2016, 4:234
41
[42]. Lawrence K., Pawan K., Amarendra N., Manoranjan K. Int. Nano Let., 2013, 8:1
42
[43]. El-Okr M.M., Salem M.A., Salim M.S., El-Okr R.M., Ashoush M., Talaat H.M. J. Magn. Magn. Mater., 2011, 323:920
43
[44]. Radhika B., Sahoo R., Srinath S. AIP Conf. Proc., 2015, 1665:1
44
[45]. Hong R.Y., Ren Z.Q., Han Y.P., Li H.Z., Zheng Y., Ding J. Chem. Eng. Sci., 2007, 6:5912
45
[46]. Ghasemi E., Mirhabibi A., Edrissi M. J. Magn. Magn. Mater., 2008, 320:2635
46
[47]. Yang C., Yu M., Zhao S., Tian Y., Bian X. Nanoscale Res. Lett.,2018, 13:378
47
ORIGINAL_ARTICLE
An efficient removal of methyl green dye by adsorption onto new modified chitosan Schiff base
New modified chitosan Schiff base (EP-CS-SB) composite was prepared from the reaction of chitosan, epichlorohydrin and trans-cinnamaldehyde (molar ratio 1:1:1) and characterized by Fourier-transform infrared spectroscopy (FT-IR), ultraviolet–visible spectroscopy (UV-Vis), thermogravimetry and differential thermal analysis (TG-DTA), differential scanning calorimetry (DSC), X-ray diffraction (XRD) and scanning electron microscope (SEM) analysis. It was applied as a new adsorbent for removal of methyl green (MG) dye. The effects of different significant parameters, such as pH solution (2-10), adsorbent dosage (0.005, 0.01 and 0.02 g) and contact time (0 – 120 min) were explored. Results show that the adsorption process was depended on pH solution. The highest adsorption capacity of EP-CS-SB was obtained 98.47% at pH =8, 120 min, and 0.02 g of EP-CS-SB. EP-CS-SB was found to be a suitable candidate for removal of cationic dye.
https://www.ajnanomat.com/article_135684_6921b14b4ba386abec34a2b63ba1d6fd.pdf
2021-10-01
274
281
10.26655/AJNANOMAT.2021.4.3
Epichlorohydrin
Cinnamaldehyde
Chitosan Schiff base
Methyl green removal
Zahra
Bashandeh
a.bashandeh@yahoo.com
1
Department of Chemistry, Faculty of Science, Golestan University, Gorgan, Iran
AUTHOR
Aliakbar
Dehno Khalaji
alidkhalaji@yahoo.com
2
Department of Chemistry, Faculty of Science, Golestan University, Gorgan, Iran
LEAD_AUTHOR
[1]. Pandey G., Singh D., Hitkari G. Int Nano Lett., 2018, 8:111
1
[2]. Rahmi., Ismaturrahmi., Mustafa I. Microchem J., 2019, 144:397
2
[3]. Yang D., Qiu L., Yang Y. J Chem Eng Data, 2016, 61:3933
3
[4]. Cinar S., Kaynar U.H., Aydemir T., Kaynar S.C., Ayvacikli M. Int J Biol Macromol., 2017, 96:459
4
[5]. Razzaz A., Ghorban S., Hosayni L., Irani M., Aliabadi M. J Taiwan Inst Chem Eng., 2016, 58:333
5
[6]. Saad A.H.A., Azzam A.M., El-Wakeel S.T., Mostafa B.B., Abd El-latif M.B. Environ Nanotech Mon Manag., 2018, 9:67
6
[7]. Kornaros M., Kyberatos G. J Haz Mater., 2006, 136:95
7
[8]. Wang K., Guo J., Yang M., Junji H., Deng R. J Haz Mater, 2009, 162:1243
8
[9]. Yagub M.T., Sen T.K., Afroze S., Ang H.M. Adv Coll Interface Sci., 2014, 209:172
9
[10]. Wang J., Shao X., Zhang Q., Tian G., Ji X., Bao W. J Mol liq., 2017, 24b8:13
10
[11]. Ke P., Zeng D., Xu K., Cui J., Li X., Wang G. ACS Omega, 2020, 5:24700
11
[12]. Zhai L., Bai Z., Zhu Y., Wang B., Luo W. Chin J Chem Eng., 2018, 26:657
12
[13]. Vakili M., Rafatullah M., Salamatinia B., Abdullah A.Z., Ibrahim M.Z., Tan K.B., Gholami Z., Amouzegar P. Carbohydr Polym., 2014, 113:115
13
[14]. Yuvaraja G., Chen D.Y., Pathak J.L., Long J., Subbaiah M.V., Wen J.C., Pan C.L. Int J Biol Macromol., 2020, 146:1100
14
[15]. Moradnia F., Taghavi Fardood S., Ramazani A., Min B.K., WooJoo S., Varma R.S. J Cleaner Prod., 2021, 288:125632
15
[16]. Ajormal F., Moradnia F., Taghavi Fardood S., Ramazani A. J Chem Rev., 2020, 2:90
16
[17]. Taghavi Fardood S., Moradnia F., Ghalaichi A.H., Danesh Pajouh S., Heidari M., Nonochem Res., 2020, 5:69
17
[18]. Sahoo J.K., Konar M., Rath J., Kumar D., Sahoo H., Sep Sci Technol., 2020, 55:415
18
[19]. Yin W., Hao S., Cao H., RSC Adv., 2017, 7:4062
19
[20]. Mahmoodi N.M., Mat Res Bull., 2013, 48:4255
20
[21]. Alizadeh N., Mahjoub M., J Nanoanalysis, 2017, 4:8
21
[22]. Taghavi Fardood S., Moradnia F., Moradi S., Forootan R., Yekke Zare F., Heidari M., Nanochem Res., 2019, 4:140
22
[23]. Yuvaraja G., Pang Y., Chen D.Y., Kong L.J., Mehmood S., Subbaiah M.V., Rao D.S., Pavuluri C.M., Wen J.C., Reddy G.M. Int J Biol Macromol., 2019, 136:177
23
[24]. Matinez-Mejia G., Vazquez-Torres N.A., Castell-Rodriguez A., del Rio J.M., Corea M., Jimenez-Juarez R. Coll Surf A, 2019, 579:123658
24
[25]. Yan Y., Yuvaraja G., Liu G., Kong L., Guo K., Reddy G.M., Zyryanov G.V. Int J Biol Macromol., 2018, 117:1305
25
[26]. Sanati M., Khalaji A.D., Mokhtari A., Keyvanfard M. Prog Chem Biochem Res., 2021, 4:319
26
[27]. Bashandeh Z., Khalaji A.D. Adv J Chem A, 2021, 4:270
27
[28]. Foroughnia A., Khalaji A.D., Kolvari E., Koukabi N. Int J Biol Macromol., 2021, 177:83
28
[29]. Lal S., Arora S., Kumar V., Rani S., Sharma C., Kumar P. J Therm Anal Calorim., 2018, 132:1707
29
[30]. Hassan M.A., Omer A.M., Abbas E., Baset W.M., Tamer T.M. Sci Rep., 2018, 8:11416
30
[31]. Azmi W., Sani R.K., Banerjee U.C. Microb Technol., 1998, 22:185
31
[32]. Fleischmann C., Lievenbrück M., Ritter H. Polymers, 2015, 7:717
32
[33]. Maghni A., Ghelamallah M., Benghalem A. Acta Phys Pol A, 2017, 132:448
33
[34]. Rida K., Chaibeddra K., Cheraitia K. Ind J Chem Technol., 2020, 27:51
34
[35]. Lamia M., Fatiha D., Bouchekara., Ayada D. Orient J Chem., 2016, 32:171
35
[36]. Vergas-Rodriquez Y.M., Obaya A., Garcia-Petronilo J.E., Vergas-Rodriquez G.I., Gomez-Cortes A., Tavizon G., Chavez-Carvayar J.A. Am J Nanomater., 2021, 9:1
36
[37]. Abbas M., Aksil T., Trari M. Desal Water Treat., 2018, 125:93
37
[38]. Mahmoud N.M.R., El-Moselhy M.M., Alkhaldi M.A. Desal Water Treat., 2019, 258:385
38
[39]. Baghat M., Farghali A.A., El-Rouby W., Khedr M., Mohassab-Ahmed M.Y. App Nanosci., 2013, 3:251
39
ORIGINAL_ARTICLE
Efficient protocol for the production of pyrimido[4,5-b] quinolines using an organic-inorganic hybrid catalyst
In this work, an efficient protocol for the synthesis of pyrimido[4,5-b]quinolines was reported. The one-pot multi-component reaction of arylaldehydes, barbituric acid (or 2-thiobarbituric acid) and anilines in the presence of an organic-inorganic hybrid material namely tetramethyl-N-(silica-n-propyl)-N′-sulfonic acid-ethylenediaminium chloride/mesylate ([TSSECM]) afforded the mentioned compounds. This protocol has several advantages including, high yields (86-95%), relatively short reaction times (110-120 min), recyclability of the catalyst and easy purification of the products without column chromatography.
https://www.ajnanomat.com/article_136239_670d7eac88dc96b322fcb78819d4c38d.pdf
2021-10-01
282
289
10.26655/AJNANOMAT.2021.4.4
Pyrimido[4,5-b]quinoline
Organic-inorganic hybrid catalyst N,N,N′,N′-Tetramethyl-N-(silica-n-propyl)-N′-sulfonic acid-ethylenediaminium chloride/mesylate ([TSSECM]) Multi-component reaction
Manije
Dianat
dianat_61@yahoo.com
1
Department of Chemistry, Payame Noor University, PO Box 19395-3697, Tehran, Iran
AUTHOR
Abdolkarim
Zare
abdolkarimzare@yahoo.com
2
Department of Chemistry, Payame Noor University, PO Box 19395‐3697 Tehran, Iran
LEAD_AUTHOR
Monavvar
Hosainpour
nooraniii@yahoo.com
3
Department of Chemistry, Payame Noor University, PO Box 19395-3697, Tehran, Iran
AUTHOR
[1]. Nikoorazm M., Khanmoradi M., Mohammadi M. Appl. Organometal. Chem., 2020, 34:e5504
1
[2]. Pourkazemi A., Nasouri Z., Fakhraie F., Razzaghi A., Parhami A., Zare A. Asian J. Nanosci. Mater., 2020, 3:131
2
[3]. Kumari P., Yadav R., Bharti R., Parvin T. Mol. Divers., 2020, 24:107
3
[4]. Majidi Arlan F., Javahershenas R., Khalafy J. Asian J. Nanosci. Mater., 2020, 3:238
4
[5]. Kumari S., Kumar D., Gajaganti S., Srivastava V., Singh S. Synth. Commun., 2019, 49:431
5
[6]. Ezzatzadeh E., Sheikholeslami-Farahani F., Yadollahzadeh K., Rezayati S. Comb. Chem. High Throughput Screen., 2021, 24:1465
6
[7]. Nabi Bidhendi G., Mehrdadi N., Firouzbakhsh M. Chem. Methodol., 2021, 5:271
7
[8]. Huang P., Chen Y., Lin H., Yu L., Zhang L., Wang L., Zhu Y., Shi J. Biomaterials, 2017, 125:23
8
[9]. Zhang B., Zhang Y., Wang Z., Yang D., Gao Z., Wang D., Guo Y., Zhu D., Mori T. Dalton Trans., 2016, 45:16561
9
[10]. Zare A., Dianat M., Eskandari M.M. New J. Chem., 2020, 44:4736
10
[11]. Sajjadifar S., Amini I., Habibzadeh S., Mansouri G., Ebadi E. Chem. Methodol., 2020, 4:624
11
[12]. Zafari S., Ghorbani-Vaghei R., Alavinia S. Mater. Chem. Phys., 2021, 270:124840
12
[13]. Sajjadifar S., Amini I., Mansouri G., Alimohammadi S. Eurasian Chem. Commun., 2020, 2:626
13
[14]. Khazaei A., Gohari-Ghalil F., Tavasoli M., Rezaei-Gohar M., Moosavi-Zare A.R. Chem. Methodol., 2020, 4:543
14
[15]. Zare A., Atashrooz J., Eskandari M.M. Res. Chem. Intermed., 2021, 47:1349
15
[16]. Ezzatzadeh E. Asian J. Nanosci. Mater., 2021, 4:125
16
[17]. A. Sadeghi Meresht, E. Ezzatzadeh, B. Dehbandi, M. Salimifard, R. Rostamian, Polycycl. Arom. Compd. in press, doi: 10.1080/10406638.2021.1913426
17
[18]. Ezzatzadeh E., Zamani Hargalani F., Shafaei F. Polycycl. Arom. Compd., in press, doi: 10.1080/10406638.2021.1879882
18
[19]. Althuis T.H., Moore P.F., Hess H.J. J. Med. Chem., 1979, 22:44
19
[20]. El-Sayed O.A., El-Baih F.M.E., El-Aqeel S.I., Al Bassam B.A., Hussein M.E. Boll. Chem. Farmac., 2002, 141:461
20
[21]. Nargund L.V.G., Badiger V.V., Yarnal S.M. J. Pharm. Sci., 1992, 81:365
21
[22]. Ghorab M.M., Ragab F.A., Heiba H.I., Arafa R.K., El-Hossary E.M. Eur. J. Med. Chem., 2010, 45:3677
22
[23]. El-Gazzar A.B.A., Hafez H.N., Nawwar G.A.M. Eur. J. Med. Chem., 2009, 44:1427
23
[24]. Abbas H.A.S., Hafez H.N., El-Gazzar A.-R.B.A. Eur. J. Med. Chem., 2011, 46:21
24
[25]. Khalafi-Nezhad A., Sarikhani S., Shaikhi Shahidzadeh E., Panahi F. Green Chem., 2012, 14:2876
25
[26]. Mohire P.P., Patil R.B., Chandam D.R., Jadhav S.J., Patravale A.A., Kumbhar D.R., Ghosh J.S., Deshmukh M.B. Res. Chem. Intermed., 2017, 43:7013
26
[27]. Reddy S.S., Reddy M.V.K., Reddy P.V.G. ChemistrySelect, 2018, 3:4283
27
[28]. Mosslemin M.H., Zarenezhad E., Shams N., Soltani Rad M.N., Anaraki-Ardakani H., Fayazipoor R. J. Chem. Res., 2014, 38:169
28
[29]. Nongthombam G.S., Nongkhlaw R. Synth. Comun., 2018, 48:541
29
[30]. Nongthombam G.S., Kharmawlong G.K., Kumar J.E., Nongkhlaw R. New J. Chem., 2018, 42:9436
30
ORIGINAL_ARTICLE
The ability of Tragopogon graminivorous DC edible medicinal plant for optimum synthesis of zinc oxide green nanoparticles and evaluation of antibacterial properties of its extract and nanoparticles
In recent years, the green synthesis of nanoparticles has become an environment-friendly method developed significantly. In this method, plant extract as a reductive and stabilizing agent plays a key role in the synthesis of nanoparticles. In this study, the optimum conditions for the green synthesis of ZnO nanoparticles are investigated using the extract of Tragopogon graminivorous DC edible-medicinal plants. Also, the antioxidant effect of the plant extract and antibacterial properties of nanoparticles and extract are evaluated. After preparation of the aqueous extract, its antioxidant properties were evaluated by the DPPH method. Then, parameters such as pH, zinc acetate dihydrate concentration, the volume of plant extract, temperature, and time were optimized. The green nanoparticles were characterized by UV-Vis, FT-IR, X-ray diffraction, and scanning electron microscope techniques. Finally, antibacterial properties of extract and biosynthesized ZnO nanoparticles were investigated. The results of the DPPH method showed that plant extract can be used as a reductive agent. Overall, it can be said that the presence of various chemical compounds that have caused the antioxidant properties of plant extract demonstrate the ability of the extract as a source of natural antioxidants. Also, plant extract and nanoparticles can be regarded as antibacterial agents.
https://www.ajnanomat.com/article_137450_0a6d55ea28a8c7da3401ad498e3f33d3.pdf
2021-10-01
290
308
10.26655/AJNANOMAT.2021.4.5
Tragopogon graminifolius DC Edible
medicinal plant Zinc oxide nanoparticles Antibacterial properties Optimal conditions
Marzieh
Naderi
marziehnaderi@yahoo.com
1
Department of chemistry, Khorramabad Branch, Islamic Azad University, Khorramabad, Iran
AUTHOR
Ghazaleh
Kouchakzadeh
gh_kouchakzadeh@yahoo.com
2
Department of chemistry, Khorramabad Branch, Islamic Azad University, Khorramabad, Iran
LEAD_AUTHOR
[1]. Nithya K., Kalyanasundharam S. OpenNano, 2019, 4:100024
1
[2]. Noorjahan C.M. Asian Journal of Pharmaceutcal and Clinical Research, 2019, 12:106
2
[3]. Saptarshi S.R., Duschl A., Lopata A.L. Journal of nanobiotechnology, 2013, 11:1
3
[4]. Faddah L.M., Abdel Baky N.A., Al-Rasheed N.M., Al-Rasheed N.M., Fatani A.J., Atteya M. BMC Complement Altern Med., 2012, 12:60
4
[5]. El Shemy M.A., Ibrahim Azab N., Fawzy Salim R. Biophysics & Molecular Biology., 2017, 2:1
5
[6]. Sperling R.A., Zhang F., Zanella M., Parak W.J. Chemical Society Reviews., 2008, 37:1896
6
[7]. Shobha N., Nanda N., Giresha A.S., Manjappa P., Dharmappa K.K., Nagabhushana B.M. Materials Science and Engineering: C., 2019, 97:842
7
[8]. Shankar S.S., Rai A., Ahmad A., Sastry M. Journal of Colloid and Interface Science., 2004, 275:469
8
[9]. Gour A., Kumar Jain N. Nanomedicine, and Biotechnology, 2019, 47:844
9
[10]. Mali V.C., Ranger K., Lavate R.A., Kumbhar D.A., Sathe S.S., Kokare B.N. Proceeding of Internatinal Conference on Advances in Materials Science, 2016, 24:648
10
[11]. Sumner L.W., Lei Z., Nilolau B.J., Saito K. Natural Product Reports., 2015, 32:212
11
[12]. Agarwal H., Venkat Kumar S., Rajeshkumar S. Resource- Efficient Technologies, 2017, 3:406
12
[13]. Santhoshkumar J., Venkat Kumar S., Rajesshkumar S. Resource-Efficient Technologies, 2017, 3:459
13
[14]. Ezzatzadeh E., Hossaini Z., Varasteh Moradi A., Salimifard M., Afshari-Sharif Abad S. Canadian Journal of Chemistry, 2019, 97:1
14
[15]. Heidari M., Bahramsoltani R., Abdolghaffari A.H., Rahimi R., Esfandyari M., Baeeri M., Hassanzadeh G., Abdollahi M., Farzaei M.H. Journal of Traditional and Complementary Medicine, 2019, 9:54
15
[16]. Formisano C., Rigano D., Senatore F., Bruno M., Rosselli S. Natural Product Research, 2010, 24:663
16
[17]. Sareedenchai V., Ganzera M., Ellmerer E.P., Lohwasser U., Zidorn C. Biochemical Systematics and Ecology, 2009, 37:234
17
[18]. Farzaei M.H., Khazaei M., Abbasabadi Z., Feyzmahdavi M., Mohseni G.R. Iranian Red Crescent Medical Journal, 2013, 15:813
18
[19]. Goorani S., Morovvati H., Seydi N., Zangeneh A., Zangeneh M.M. Comparative Clinical Pathology, 2019, 28:435
19
[20]. Feyzmahdavi M., Khazaei M., Gholamin B., Abbasabadi Z. Journal of Reports in Pharmaceutical Sciences, 2017, 6:161
20
[21]. Sadeghi A., Bahramsoltani R., Rahimi R., Farzaei M.H., Farzaei F., Minoosh Z., Haghghi S., Abdollahi M. Journal of Dietary Supplements, 2018, 15:197
21
[22]. Farzaei M.H., Ghasemi-Niri S.F., Abdolghafari A.H., Baeeri M., Khanavi M., Navaei-Nigjeh M., Abdollahi M., Rahimi R. Pharmaceutical Biology, 2015, 53:429
22
[23]. Zangeneh M.M., Salmani S., Zangeneh A., Khedri R., Zarei M.S. Comparative Clinical Pathology, 2019, 28:1197
23
[24]. Al-Rimawi F., Rishmawi S., Ariqat Sh.H., Khalid M.F., Warad E., Salah Z. Complementary and Alternative Medicine, 2016, 2:1
24
[25]. Seifpour R., Nozari M., Pishkar L. Journal of Inorganic and Organometallic Polymers and Materials, 2020, 30:2926
25
[26]. Kroschewsky J.R., Mabry T.J., Markham K.R., Alston R.E. Phytochemistry, 1969, 8:1495
26
[27]. Kucekova Z., MLcek J., Humpolicek P., Rop O., Valasek P., Saha P. Molecules, 2011, 16:9207
27
[28]. Farzaei M.H., Rahimi R., Attar F., Siavoshi F., Saniee P., Hajimahmoodi M., Mirnezami T., Khanavi M. Natural Product Communication, 2014, 9:121
28
[29]. Britton H.T.S., Robinson R.A. Journal of the Chemical Society (Resumed), 1931, 0:1456
29
[30]. Brand-Williams W., Cuvelier M.E., Berset C. LWT- Food Science and Technology, 1995, 28:25
30
[31]. Katalinik V., Milos M., Kulisic T., Jukic M. Food Chemistry, 2006, 94:550
31
[32]. Choi C.W., Kim S.C., Hwang S.S., Choi B.K., Ahn H.J., Lee M.Y., Park S.H., Kim S.K. Plant Science, 2002, 163:1161
32
[33]. Behravan M., Hossein Panah A., Naghizadeh A., Ziaee M,. Mahdavi R., Mirzapour A. International Journal of Biological Macromolecules, 2019, 124:148
33
[34]. Seifi Mansour S., Ezzatzadeh E., Safarkar R. Asian Journal of Green Chemistry, 2019, 3:353
34
[35]. Villanueva M.E., Cuestas M.L., Pérez C.J, Dall´ Orto V.C., Copello G.J. Journal of Colloid and Interface Science, 2019, 536:372
35
[36]. Baek S., Hee Joo S., Toborek M. Journal of Hazardous Materials, 2019, 373:122
36
[37]. Iravani S., Green Chemistry., 2011, 13:2638
37
[38]. Jamzad M., Karami Bidkorpeh M. Journal of Nanostructure in Chemistry, 2020, 10:193
38
[39]. Hosseini Koupaei M., Shareghi B., Saboury A. A., Davat F., Semnani A., Evini M. Royal Society of Chemistry Advances, 2016, 6:42313
39
[40]. Marja P., Hopia A.I., Vuorela H.J., Rauha J., Pihlaja K., Kujala T.S., Heinonen M. Journal of Agriculture Food Chemistry, 1999, 47:3954
40
[41]. Blainski A., Lopes G.C., Palazzo de Mello J. C. Molecules, 2013, 18:6852
41
[42]. Li X., Wu X., Huang L. Molecules, 2009, 14:5349
42
[43]. Chandra Shekhar T., Anju G. American Journal of Ethnomedicine, 2014, 1:244
43
[44]. Huong D.Q., Duong T., Cam Nam P. Vietnam Journal Chemistry, 2019, 57:469
44
[45]. Ansari M.A., Murali M., Prasad D., Alzohairy M.A., Almatroudi A., Alomary M.N., Udayashankar A.C., Singh S.B., Asiri S.M., Ashwini B.S., Gowtham H.G., Kalegowda N., Amruthesh K.N., Lakshmeesha T.R., Niranjana S.R. Biomolecules, 2020, 10:336
45
[46]. Ambrožič G., Crnjak Oral Z., Žigon M., Materials and technology, 2011, 43:173
46
[47]. Ezealisiji K.M., Siwe-Noundou X., Maduelosi B., Nwachukwu N., Maçedo Krause R. W. International Nano Letters, 2019, 9:99
47
[48]. Basnet P., Inakhunbi Chanu T., Samanta D., Chatterjee S. Journal of Photochemistry and Photobiology, 2018, 183:201
48
[49]. Malek Mohammadi F., Ghasemi N. Journal of Nanostructure in Chemistry, 2018, 8:93
49
[50]. Jain P.K., Huang X., El-Sayed I.H., El-Sayed M. A. Plasmonics, 2007, 2:107
50
[51]. Khalil M.M.H., Ismail E.H., El-Baghdady K.Z., Mohamed D. Arabian Journal of Chemistry, 2014, 7:1131
51
[52]. Buazar F., Bavi M., Kroushawi F., Halvani M., Khaledi-Nasab A., Hossieni S.A. Journal of Experimental Nanoscience, 2016, 11:175
52
[53]. Rafaie H., Samat N., Nor R.M. Materials Letters, 2014, 137:297
53
[54]. Moezzi A., Cortie M., Mc Donagh A. Royal Society of Chemistry, 2011, 40:4871
54
[55]. Rodríguez-Paéz J.E., Caballero A.C., Villegas M., Moure C., Durán P., Fernández J.F. Journal of the European Ceramic Society, 2001, 21:925
55
[56]. Nithya K., Kalyanasundharam S. Open Nano, 2019, 4:100024
56
[57]. Dinesh V.P., BiJi P., Ashok A., Dhara S.K., Kamaruddin M., Tyagi A.K., Raj B. Electronic Supplementary Material (ESl) for RSC Advances, 2014, 4:58930
57
[58]. Bouzourâa M., En Naciri A., Moadhen A., Rinnert H., Guendouz M., Battie Y., Chaillou A., Zaïbi M.A. Materials Chemistry and Physics, 2016, 175:233
58
[59]. Nagarajan S., Kuppusamy K.A. Journal of Nanobiotechnology, 2013, 11:39
59
[60]. Gnanasangeetha D., Thambavani D.S. Journal of Chemical, Biological and Physical Sciences, 2014, 4:238
60
[61]. Wasly H.S., El-Sadek M.S.A., Henini M. Applied Physics A: Materials Science & Processing, 2018, 124:76
61
[62]. Wang Z.L. ACS Nano, 2008, 2:1987
62
[63]. Debanath M.K., Karmakar S. Materials Letters, 2013, 111:116
63
[64]. Pudukudy M., Yaakob Z. Journal Cluster Science, 2014, 26:1187
64
[65]. Charles K. Introduction to Solid States Physics. Eighth Edition, New York: Wiley, 2005
65
[66]. Singh J., Kaur S., Kaur G., Basu S., Rawat M. Green Process Synthesis, 2019, 8:272
66
[67]. Bouazza A., Bassaid S., Daho B., Messori M., Dehbi A. Polymers and Polymer Composites, 2021, 29:417
67
[68]. Thi T.U.D., Nguyen T.T., Thi Y.D., Thi K.H.T., Phan B.T., Pham K.N. Royal Society of Chemistry Advances, 2020, 10:23899
68
[69]. Awwad A.M., Amer M.W., Salem N.M., Abdeen A.O. Chemistry International, 2020, 6:151
69
[70]. Pillai A.M., Sivasankarapillai V.S., Rahdar A., Joseph J., Sadeghfar F., Anuf A.R., Rajesh K., Kyzas G. Journal of Molecular Structure, 2020, 1211:128107
70
[71]. Fahimmunisha B.A., Ishwarya R., AlSalhi M.S., Devanesan S., Govindarajan M., Vassehran B. Journal of Drug Delivery Science and Technology, 2020, 55:101465
71
[72]. Yusof H.M., Mohamah R., Zaidan U.H., Abdul Rahman N.A. Journal of Animal Science and Biotechnology, 2019, 10:57
72
[73]. Zhang L., Jiang Y., Ding Y., Daskalakis N.N., Jeuken L.J.C., Povey M.J., Ơ Neill A.J., York D.Y. Journal of Nanoparticle Research, 2010, 12:1625
73
[74]. Vijayakumar S., Arulmozhi P., Kumar N., Sakthivel B., Prathip Kumar S., Praseetha P.K. Materials Today: Proceedings, 2019, 23:73
74
[75]. Ahmar Rauf M., Owais M., Rajpoot R., Ahmad F., Khan N., Zubair S. Royal Society of chemistry Advsnced, 2017, 7:36361
75
ORIGINAL_ARTICLE
Synthesis, structural evaluation of molybdenum oxide (MoO3) nanoparticles and its application as CO2 gas sensor
In the present study we report a simple eco-friendly hydrothermal protocol for the synthesis of molybdenum oxide (MoO3) nanoparticles at various temperatures i.e., 80-200 °C at intervals of 20 °C designated as S1-S6 sequentially with time duration of 4 h for each batch. The synthesized samples were characterized by X-Ray Fluorescence (XRF), X-Ray Diffraction (XRD), Fourier Transform Infra-red (FTIR), UV- Visible Diffuse Reflectance (UV-Vis DRS), Laser Raman, Cyclic Voltammetry (CV), X-Ray Photoelectron Spectroscopy (XPS) and Transmission Electron Microscopy (TEM) to find out their elemental composition, structure, morphology and the optical band gap. The XRD analysis indicates well-crystallized orthorhombic structure with preferred orientation along (210) plane. The presence of O-Mo-O stretching vibration was observed by FTIR analysis The gas sensing studies were carried out to examine the material’s Sensitivity over a temperature range of 50oC to 400oC for various gas concentrations i.e. 200-1000 ppm of CO2 gas. The sensor had a Sensitivity of S=68.5% for S4 sample at an optimum temperature of 200 °C. The adsorption of desired gas on the material correlated well with the particle size of material at different temperature. The response and recovery times were 50 s and 40 s respectively.
https://www.ajnanomat.com/article_137598_12b16f8fc0847e79c4f69950d954d767.pdf
2021-10-01
309
320
10.26655/AJNANOMAT.2021.4.6
MoO3 Nanoparticles
Hydrothermal protocol
XRD
XPS
TEM
M.V.
Manasa
mv_manasa@yahoo.com
1
Polymer and Functional Materials Division, CSIR-Indian Institute of Chemical Technology (CSIR-IICT), Habsiguda, Hyderabad -500007, India
AUTHOR
G. Sarala
Devi
sarala@csiriict.in
2
Polymer and Functional Materials Division, CSIR-Indian Institute of Chemical Technology (CSIR-IICT), Habsiguda, Hyderabad -500007, India
LEAD_AUTHOR
[1]. Zhenfeng B., Takashi T., Peng Z., Mamoru F., Tetsuro M. Nature Communications, 2014, 5:30
1
[2]. Lee C.Y., Li S.Y., Lin P., Tseng T.Y. IEEE Trans. Nanotechnol., 2006, 5:216
2
[3]. Li S.Y., Lin P., Lee C.Y., Tseng T.Y. J. Appl. Phys., 2004, 95:3711
3
[4]. Bai S.N., Tseng T.Y., Thin Solid Films, 2006, 515:872
4
[5]. Wang Z., Song J. Science, 2006, 312:242
5
[6]. He H. Jr., Hsin C.L., Liu J., Chen L.J., Wang Z.L. Adv. Mater., 2007, 19:781
6
[7]. Ra H.W., Choi K.S., Kim J.H., Hahn Y.B., Im Y.H. Small, 2008, 4:1105
7
[8]. Kosta P., Giorgos A., Dimitrios A., Ahmed M., Umar D., Ioannis T., William I. M., Arokia N. and George A. Appl. Phys. Lett., 2020, 116:163505
8
[9]. Marabelli F., Parraviciny G.B., Drioli F.S. Phys. Rev. B., 1995, 52:1433
9
[10]. Chen J., Deng S.Z., She J.C., Xu N.S., Zhang W.X., Wen X.G., Yang, S.H. J. Appl. Phys., 2003, 93:1744
10
[11]. Chowdhuri A., Gupta V., Sreenivas K., Kumar R., Mozumdar S., Patanjali P.K. Appl. Phys. Lett., 2004, 84:1180
11
[12]. Madhuri M., Subrata K., Sujit Kumar G., Sudipa P., Tapan K. S., Yusuf S.M., Tarasankar P. J. Collo. Inter. Sci., 2005, 286:187
12
[13]. Beek B.W.J.E., Slooff L.H., Wienk M.N., Kroon J.M., Janseen R.A.J. Adv. Funct. Mater., 2005, 15:1703
13
[14]. Sheng X., Zhong L.W. Nano Res., 2011, 4:1013
14
[15]. Olson D.C., Piris J., Colins R.T., Shaheen S.E., Ginley D.S. Thin Solid Films, 2006, 496:26
15
[16]. Xu Z.X., Roy V.A.L., Stallinga P., Muccini M., Toffanin S., Xiang H.F., Che C.M. Appl. Phys. Lett., 2007, 90:223505
16
[17]. Fernandes D.M., Silva R., Winkler Hechenleitner A.A., Radovanovic E., Custódio Melo M.A., Gómez Pineda E.A., Mater. Chem. Phy., 2009, 115:110
17
[18]. Jian F.L., Li B.L., Xue H.S., Kai D., Jing N., Chao J.L., Wei S.L. Langmuir, 2013, 29:13975
18
[19]. Barsan N., Weimar U., J. Phys. Condens. Matter., 2003, 15:813
19
[20]. Yamazoe N., Shimanoe K. J. Sens., 2009, 875704:21 pages
20
[21]. Sarala Devi G., Takeo H., Yasuhiro S., Makoto E. Sensors and Actuators B., 2002, 87:122
21
[22]. Tomescu A., Simion C.E., Alexandrescu R., Morjan I., Scarisoreanu M. Romanian J. Inf. Sci. & Tech. 2008, 11:85
22
[23]. Gajendiran J., Rajendran V. Materials Letters, 2014, 116:311
23
[24]. Saravanana R., Karthikeyan S., Gupta V.K., Sekaran G., Narayanan V., Stephen A. Materials Science and Engineering: C, 2013, 33:91
24
[25]. Habibi M.H., Karimi B., Zendehdel M., Habibi M. Spectrochim Acta: A Mol Biomol Spectrosc., 2013, 116:374
25
[26]. Jianyu Y., Shendong Z., Xiaoyong X., Wenchang Z., Bing F., Jingguo H. J. Materials Chemistry: A, 2015, 3:1199
26
[27]. Petetin L., Berger F., Chambaudet A., Planade R. Sensors and Actuators B: Chemical, 2001, 78:166
27
[28]. Niskanen A., Varpula A., Utriainen M., Natarajan G., Cameron D. Sensors and Actuators B: Chemical, 2010, 148:227.
28
[29]. Yadav B.C., Richa S., Dwivedi C.D., Pramanik P., Sensors and Actuators B: Chemical, 2008, 131:216
29
[30]. Manasa M.V., Sarala Devi G., Prasada Reddy P.S., Sreedhar B. Materials Research Express, 2019, 6:125041
30
[31]. Rosetti R., Nakahara S., Brus L.E. Journal of Chemical Physics, 1983, 79:1086
31
[32]. Hübner M., Sinion C., Haensch A., Barsan N. and U. Sensors and Actuators B: Chemical, 2010 151:103
32
[33]. Ganguly A., George R. Bulletin of Materials Science, 2007, 30:183
33
[34]. Nagabhushana G.P., Samrat D., Chandrappa G.T. RSC Advances, 2014, 4:56784
34
[35]. Arumugam M., Gang-Juan L., Chin-Yi C., Jing-Heng C. Materials Research Bulletin, 2015, 62:184
35
[36]. Manasa M.V., Prasada Reddy P.S., Adi Narayana Reddy B., Sarala Devi G. Journal of Advanced Physics, 2018, 7:1
36
ORIGINAL_ARTICLE
Synthesis and characterization of curcumin nanoparticles by hydrothermal method
Curcumin (CRM) is a phytochemical that has potent antiproliferative effects against a variety of tumors in vitro. Curcumin, however, is limited in its clinical utility due to its poor solubility. Hydrothermal synthesis is a novel method that yields nanoparticles with narrow particle size distribution and high purity without further treatment the use of toxic solvents. Nanosized CRM with the average particle size of 186.2 nm was prepared by a simple hydrothermal process to enhance the aqueous solubility of CRM. Differential scanning calorimetry (DSC) and X-ray diffraction (XRD) analysis identifies that the particles are highly crystalline and revealed no polymorphic changes in CRM on hydrothermal treatment and scanning electron microscopy (SEM) identified that the CRM nano agglomerates. Zeta potential (ZP) results demonstrated the relative stability of nanosized CRM after hydrothermal treatment. Nanosized CRM particles exhibited greater solubility and hence dissolution rate as compared to the original drug. The present study offers a simple process that lacks the use of organic solvent, therefore, is green, and had good yield being a single-step process, to synthesize and to design nanosized CRM for better drug delivery applications.
https://www.ajnanomat.com/article_139267_4cf61ddc4fcb473dd31ad9fe9209104a.pdf
2021-10-01
321
330
10.26655/AJNANOMAT.2021.4.7
Nanoparticles
Hydrothermal
curcumin
Solubility
Kisan
Patel
hsmahajan@rediffmail.com
1
R.C. Patel Institute of Pharmaceutical Education and Research Shirpur, Dist. Dhule, India
AUTHOR
Sachin
Chandankar
smchandankar18@gmail.com
2
R.C. Patel Institute of Pharmaceutical Education and Research Shirpur, Dist. Dhule, India
AUTHOR
Hitendra
Mahajan
hsmahajan77@gmail.com
3
R.C. Patel Institute of Pharmaceutical Education and Research Shirpur, Dist. Dhule, India
LEAD_AUTHOR
[1] . Charitidis C.A., Georgiou P., Koklioti M.A., Trompeta A.F., Markakis V. Manuf Rev., 2014, 1
1
[2] . Darr J.A., Poliakoff M. Chem Rev., 1999, 99:495
2
[3]. Gribov E.N., Parkhomchuk E.V., Krivobokov I.M., Darr J.A., Okunev A.G. J Memb Sci., 2007, 297:1
3
[4] . Gong K., Darr J.A., Rehman I.U. Int J Pharm., 2006, 315:93
4
[5]. Gan Y.X., Jayatissa A.H., Yu Z., Chen X., Li M. J Nanomater., 2020, 2020:3 pages
5
[6]. Ismail A.A., El-Midany A., Abdel-Aal E.A., El-Shall H. Mater Lett., 2005, 59:1924
6
[7]. Franger S., Le Cras F., Bourbon C., Rouault H. Electrochem Solid-State Lett., 2002, 5:231
7
[8]. Abdel-Aal E.A., Malekzadeh S.M., Rashad M.M., El-Midany A.A., El-Shall H. Powder Technol., 2007, 171:63
8
[9]. Abdel-Aal E.A., El-Midany A.A., El-Shall H. Mater Chem Phys., 2008, 112:202
9
[10]. Shah V.P., Amidon G.L., Lennernas H., Shah V.P., Crison J.R. AAPS J., 2014, 16:894
10
[11]. Gu Z., Wu A., Li L., Xu Z.P. Pharmaceutics, 2014, 6:235
11
[12]. Li C, Ge X, Li G, Gao Q, Ding R. Adv Powder Technol., 2014, 25:1661
12
[13]. Abraham H.A., Patel N.R., Torchilin V.P.
13
Int. J. Pharm. 2014 ,464:178
14
[14]. Keshari P., Sonar Y., Mahajan H. Mater Technol., 2019, 34:423
15
[15]. Mahajan H.S., Gattani S.G. Chem Pharm Bull., 2009, 57:388
16
[16]. Mahajan H.S., Gattani S.G., Pharm Dev Technol., 2009, 14:226
17
[17]. Gokhale J.P., Mahajan H.S., Surana S.S. Biomed Pharmacother., 2019, 112:108622
18
[18]. Patil P.H., Wankhede P.R., Mahajan H.S., Zawar L.R. Recent Pat Drug Deliv Formul., 2018, 12:53
19
[19]. Riman R.E., Suchanek W.L., Byrappa K., Chen C.W., Shuk P., Oakes C.S. Solid State Ionics., 2002, 151:393
20
[20]. Rezaei-aghdam E., Shamel A., Khodadadi-moghaddam M., Rajaei E., Mohajeri S. Asian Journal of Nanoscience., 2021, 4:188
21