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International Journal of Research in Advent Technology, Vol.7, No.6, June 2019
E-ISSN: 2321-9637
Available online at www.ijrat.org
44doi: 10.32622/ijrat.76201928

Abstract— Guar gum Nano particles are smaller in size,
due to their smaller size of exact directing, drug release
possible, improvement of salutary efficiency and decrease of
harmlessness. NPs are low-cost, biocompatible, non-toxic,
and biodegradable to chemical alterations. The guar gum
Nano particles are widely used in pharmaceuticals. This
methods also used for the preparation of Nano particles are
nonchemical, precipitation, dialysis, spray drying and
mixture of these methods. Current review focus on the
synthesis, types, preparation and characterization of Guar
gum Nano particles by Ionic gelation method and cross
linking method most advanced application related to targeted
drug delivery. Nanoparticles act as possible transfers for
some classes of cosmetics and drugs. It has been set up that
the creation of nanoparticles depends upon the molecular
mass of the galactomannan, solvent, surfactant, cross-linker
and agitation. The particle size can be determined by
scanning electron microscopy studies such as DLS, UV and
SEM. The morphology and size of the gum Nano particles are
determined by increased technique created spherical
nanoparticles of size 10–280 nm. The results are given within
the sort of tables and graphs.
Index Terms— Guar gum, Tris sodium
Trimetaphosphate, sodium hydroxide, ultrapure water, Ionic
gelation method.
I. INTRODUCTION
Guar Gum Nano particles measures
10-1000nanometres or less. The properties of many
conventional materials change when formed from
nanoparticles. This is normally as a result of nanoparticles
have a bigger extent per weight than larger particles that
causes them to be a lot of reactive to another molecules. The
size of the particle depends upon nozzle size, atomization
pressure, and spray flow, body of water air temperature and
quantity of cross linking.1
Drug delivery system notion is not
novel in the action of some syndromes. Targeting delivery of
drugs to carry a necessary dose of drug to the mark, proper
carriers of drug were required. These Nano particle carriers
have key potential application for the admin of health-giving
Manuscript revised June 4, 2019 and published on July 10, 2019
Mr.G.Muthaih, Department of Chemistry, Acharya Nagrjuna University,
Guntur,Andhrapradesh,India.
Mrs.S.Nagamani, Information Technology, Lakireddy balireddy college of
Engineering, Mylavarm, Andhrapradesh,India.
Dr.D.Ramachandran, Department of Chemistry,Acharya Nagrjuna
University,Guntur,Andhra Pradesh,India.
molecule. Lipase is mostly used enzyme in feed, food,
pharmaceutics, which can hydrolyze obese into glycerol and
full of fatty acid2, 3
. Ionic gelation (IG), also called
‗ion-induced gelation‘, ends up in small particles (MPs)
nanoparticles (NPs) and with defects like improper surface
morphology, fragile particulate system, high dispensability
index, and lack of correct surface modification sites to
connect purposeful moieties.[4—6]Nanoparticles act as
possible carries for numerous courses of drugs such as,
antihypertensive ,agents, immunomodulators, hormones and
anticancer agents.Macro molecules like proteins, nucleic
acids, antibodies and peptides.
[7-8]
O
O
OH CH2OH
OH
OHOH
HO
HOO
HOH2C
O
O
HO
H2C
STMP
Span80Glycerol
Distilled Water Continious Stirring
4 Hours
Nano Emulsion
Kept Overnight
rpm20000
Recentrifugation
30 minutes
Centrifugation
30 minutes
Cross linker
Guargum Nano Particle
rpm20000
Guargum Powder
Structure of
Guargum
NaOH
Fig 1:Systematic process of Guar gum Nano Particle
preparation based on Ionic Gelation Method
II. RELATED WORK
Nano Particles are a category of materials with diameters
within the vary from 1 to 100nm. These systems area unit
created unremarkably in nature, and that they area unit
referred to as colloids, aerosols and submicron solids; these
area unit dirt particles and suspended solids in liquid systems,
smoke, clouds and mist. Different nanoparticles area unit
deliberately created for distinctive applications in areas of
medication and physics[9-11].Fabricated metal colloids are
used for the so many years in manufacturing of glass[12-14].
PCA ways applied with numerous qualitative analysis
techniques have mature to become themedicine analysis, as
well as techniques capable of aiding within the diagnosis of
multiple diseases like breast and cervical cancer[17,18] and
leukemia [19]. GGNPs has been widly used for breast cancer
delivery to the drug unless retarding property and condition
Preparation and characterization of Guar gum Nano
Particle through DLS, UV and SEM
Gunti Muthaiah, S.Nagamani, Dr.D.Ramachandran
International Journal of Research in Advent Technology, Vol.7, No.6, June 2019
E-ISSN: 2321-9637
Available online at www.ijrat.org
45doi: 10.32622/ijrat.76201928
to microorganism degradation within the intensive. Very
little data is out there within the open literature for the chance
of exploitation gum based mostly Nano sized materials as a
drug carrier In this an attempt is formed in getting ready Nano
sized uncoated and catalyst functionalized gum NPs by ionic
gelation and cross-linking methodology. Particle size poly
dispersity index, and size was established by DLS, UV, and
SEM.
III.EXPERIMENTAL
A .Chemicals required
Guargum(Mw220kDa),Ttrisodium
trimetaphosphate,Na3P3O9 (STMP), and sodium hydroxide
(NaOH).All solutions were ready with ultrapure water.
B. Preparation
Preparation of cross-linked nanoparticles varied
amounts of GG (concentration starting from 0.05 to 0.2 %
w/v) were additional in to a 2M NaOH solution (100 ml,
pH=12.0) and were allowed to hydrate for a minimum of 2h
underneath constant magnetic stirring at temperature.A
STMP solution (100mL, concentration varied from 0.2 to
10% w/v) was then additional at a rate of flow of one mL/min
employing a peristaltic pump, and therefore the reaction
mixture was then ceaselessly stirred nightlong. The resultant
mixture dispersion was dialyzed against H2O till neutral pH
(approx.72h). An aliquot of the sample suspension was
unbroken for particle size measurements, whereas the
remaining product was freeze-dried by freeze drying then
keep in an exceedingly desiccator.
Solvent
Polymer in aqueous phase
(Guar gum)
O/W Emulsion
Nano Emulsion
Cross linked Nano particles in preparative media
Cross linked Nano particles in preparative media
Sonication Span80 (Emulsifier)
Glycerol
NaoH STMP (Cross linker) Tri sodium
trimetaphasphate
Centrifugation After that again Wash and
Centrifugation
Stirring one Complete
Night
Fig 2: Schematic representation of nano particle
preparation
Batch
GG
concentrati
on (%)
STMP
concentrati
on (%)
Size SDn
m
PD
I
GGNP 0.5 10 780±1.4 0.5
1
GGNP
2
0.5 5 460±1.3 0.4
GGNP
3
0.5 2.5 417±1.2
0.3
2
GGNP
4
0.4 1 360±1.6
0.2
8
GGNP
5
0.4 0.5 537±8.9
0.2
5
GGNP
6
0.4 0.25 450±12.4 0.2
GGNP
7
0.3 0.05 387±0.6
0.1
8
GGNP
8
0.3 0.03 593±1.3
0.1
2
GGNP
9
0.3 0.02 208±0.9
0.1
1
Table 1: Characterization of different Nanoparticle
Fig 3: STMP Concentration and PDI
C. DLS Analysis
Particle size and DLS measurements the common hydraulics
diameter of the nanoparticles determined in water at 25 °C by
dynamic lightweight scattering measurements employing a
Malvern Zeta size ZS90 (Malvern Instruments, Worcester,
UK). The same Instrument allow the determination of 3
measurements and polydispersity index (PDI). Additionally,
period of time dynamic nanoparticle image was achieved by
nanoparticle following analysis (NTA) employing a Nano
sight LM10 instrument prepared with a sample chamber with
a 532nm optical maser and a 560 nm long pass filter. The
particle size was calculated exploitation the Stokes–Einstein
0
0.1
0.2
0.3
0.4
0.5
0.6
10.00 2.50 0.50 0.05 0.02
PDI
% Concentration
International Journal of Research in Advent Technology, Vol.7, No.6, June 2019
E-ISSN: 2321-9637
Available online at www.ijrat.org
46doi: 10.32622/ijrat.76201928
Fig. 4: (b) Guar gum Nano particle Correlation function
D. UV-Vis Spectra Analysis:
The reduction of pure guar gum Nano particles was
monitored under UV–vis spectrophotometer (Thermo
scientific-Genesys10S) 3ml of sample was withdrawn .The
absorbance was measured. UV-vis spectral analysis was done
by between 300-700nm.Guar gum nanoparticles formation
and the stability of the reduced GGNPs in the filtrate were
monitored by using UV-Vis Spectrophotometer (fig. 5a and
5b). An UV-Vis Spectrophotometer is one of the most
important to determine the formation of polymer
nanoparticles. The results were plotted and Shown in Fig.6a
and 6b. The UV–Vis spectrum Showed an SPR peak of guar
gum nanoparticles at 350 nm. It as well known that shape and
size of the Guar gum nanoparticles reflects the absorbance
peak. The absorption spectrum obtained showed a strong
surface Plasmon resonance band maximum at 355 nm (fig. 5)
a characteristic peak of guar gum nanoparticles.
Fig 5: (a) Guar gum with solvent (b) after addition of
cross linker STMP
Fig.6 (a): UV-Visible spectral analysis of synthesized guar
gum nano particles without cross linker
Fig.6 (b): UV-Visible spectral analysis of synthesized
guar gum nanoparticles with cross linker (STMP)
E. SEM ANALYSIS
The scanning microscope (SEM) is one of the
foremost versatile instruments on the market for the check
and analysis of the microstructure morphology and chemical
conformation characterizations.
SURAFCE MORPHOLOGY
The surface morphology of nanoparticles was studied by
scanning microscopy employing a(SEM Jeol JSM-6060LV)
Instrument. Sample were placed on stumps, dehydrated
with chemical element Associate in Nursing covered with
golden alloy in a chemical element atmosphere (current 20
mA, pressure 10e-3 Pa (employing a coater (Quorum, Q
150RES)).
International Journal of Research in Advent Technology, Vol.7, No.6, June 2019
E-ISSN: 2321-9637
Available online at www.ijrat.org
47doi: 10.32622/ijrat.76201928
Fig.7(a) SEM Micrograph of 100nm
Fig 7(b) SEM micrograph of Guar gum Nano Particles.
Fig. 7(c) SEM Micrograph of 1µm
Fig.7(d) Guar gum particles
V.RESULT AND DISCUSSION
The scanning electron microscope (SEM) is one among the
foremost versatile instruments on the market for the
investigation and analysis of the microstructure morphology
and chemical conformation characterization. Guar gum Nano
particles were investigated by SEM as show Fig-7(a, b) The
SEM micrographs the particle size were obtained 10-100 nm
which is show in the Fig 7(a, b c d).
VI.CONCLUSION
The techniques namely DLS, UV and SEM mainly used for
morphological studies of nanoparticles. Various researchers
used these techniques to point out that the made Nano
particles were additional or less uniform in size and form.
However, challenges and also the success for the researchers
during this rising field would rely to an oversized extent on
the provision, value and simple handling and performance of
the delicate techniques delineate during this paper. Further,
the standard and extent of data derived through these
techniques i.e. DLS, ultraviolet and SEM chemical analysis,
additionally depends to an oversized extent on the extent of
understanding of the user, experience and right sample
preparation, characterization techniques for nanoparticle
employed in drug delivery application.
REFERENCES
[1] N.V.Ravi Kumar, Nano and Micro particles as controlled drug delivery
devices,JPharma Pharmaceut Sci,2000,3(2):234-258.
[2] Sunil A. Recent advances on chitosan –based macro-and nano particles
in drug delivery, Journal of controlled Release 100 (2004) 5-28.
[3] Ashutosh Kar, Text book of Pharmaceutical Drug analysis, ISBN (13),
P293-311.
[4] Patel VM, PrajapatiBG, PatelMM.Design and characterization of
chitosan-containing mucoadhesive buccal patches of propranolol
hydrochloride. Acta Pharms 2007 ;57:61-72.
[5] Badawi AA, EI-Laithy HM, EI Qidra RK, EI Mofty H,EI dally M.
Chitosan based nanocarriers for indomethacin ocular delivery. Arch
Pharm Res 2008;31:1040-
[6] T.Akagi, M.Higashi, T.Kaneko, T.Kida, M.Akashi, Bio
macromolecules 7(2006)297-303.
[7] V.P.tarchilin,pharm.RES.24(2007)1-
[8] Sperling R. A., Gil P. R., Zhang F., Zanella M., Parak W.,
―Biological applications of goldna nopartticles‖,J., Chem. Soc. Rev.,
vol.37,pp. 1896-1908,2008.
[9] Weibo C., Ting G., Hao H., Jintao S., ―Applications of gold
nanoparticles in cancer nanotechnology‖, Nanotechnology Science
Applications, I, pp. 17-32, 2008.
[10] Devika B.Ch.,Arezou A.G., Warren C.W., ―Determining the size
and shape Dependence of nanoparticle -Uptake into Mammalian
Cells‖,Nano Letters, vol. 6,pp. 662-668,2006.John M.T., Pure& Appl.
Chem., 60,pp. 1517-1528,1988.
[11] Klaus, E.; Marion, L.; Martin, M., Matthias, P.;Helmut, S., Method for
manufacturing substrates with transparent and color coating stable at
International Journal of Research in Advent Technology, Vol.7, No.6, June 2019
E-ISSN: 2321-9637
Available online at www.ijrat.org
48doi: 10.32622/ijrat.76201928
high temperature and in the presence of ultraviolet rays,U.S. Patent,
6156388,Dec. 5, 2000.
[12] Jan J.G., ―On the relationships between SVD, KLT and PCA‖, pattern
recognition, vol. 1-6,pp.375-381,1981.
[13] Salim C., Amrane H., Boualem S., ―A new PCA-based method for data
compression and enhancement of multi-frequency polarimetric SAR
imagery‖,J. Intelligent data analysis, 6, pp. 187207,2002
[14] Mia H., Sanne E., ―Robust PCA and classification in biosciences.
[15] Pichardo J.L., Frausto C., Barbosa o., Huerta, R., Gonzalez J.L.,
Ramirez C.A., Gutierrez G., Medina C., ―Ramanspectroscopy and
multivariate analysis of serum sample form breast cancer patients‖,
Lasers Med. Sci.,22,pp. 229-236,2007.
[16] Gonzalez J.L., Rodriguez J., Martinez J.C., Frausto, C., Java L.,
Aguilar A., Vargas H., Martinez E., presented at Laser Florence 2009,
International Congress Laser Medicine with pre conference Courses,
November 6-November 7, Springer, Florence 2009,12(26):pp. 91-95.
[17] Martinez J.C., Gonzalez J.L., Frausto C., Miranda M.L., Soria C.,
Medina J., presented at Laser Florence 2008, International Congress
Laser medicine with Pre conference Courses.
AUTHOR PROFILE
Mr.Gunti Muthaiah Research scholar in department of
Chemistry at Acharya Nagarjuna University, Guntur. He
published 4 International Journals. He attended 4
national conferences. He has 7 years of teaching
experience and 5 years of Research experience.
Sikhinam Nagamani. Working as an Assistant
Professor in the department of IT, Lakireddy
Balireddy Collge of Engineering,,Mylavarm. She
attended five conferences and published 7
Interantional jornals. She has eleven years of Teaching
experience.She is a member of ISTE, CSI& IAENG
Dr.D.Ramachandran working as associate professor in
Department of chemistry at Acharya Nagarjuna
University,Guntur. He published 38 national journals
and 68 International journals. He attended 40 national
conferences and 6 International Conferences.

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76201928

  • 1. International Journal of Research in Advent Technology, Vol.7, No.6, June 2019 E-ISSN: 2321-9637 Available online at www.ijrat.org 44doi: 10.32622/ijrat.76201928  Abstract— Guar gum Nano particles are smaller in size, due to their smaller size of exact directing, drug release possible, improvement of salutary efficiency and decrease of harmlessness. NPs are low-cost, biocompatible, non-toxic, and biodegradable to chemical alterations. The guar gum Nano particles are widely used in pharmaceuticals. This methods also used for the preparation of Nano particles are nonchemical, precipitation, dialysis, spray drying and mixture of these methods. Current review focus on the synthesis, types, preparation and characterization of Guar gum Nano particles by Ionic gelation method and cross linking method most advanced application related to targeted drug delivery. Nanoparticles act as possible transfers for some classes of cosmetics and drugs. It has been set up that the creation of nanoparticles depends upon the molecular mass of the galactomannan, solvent, surfactant, cross-linker and agitation. The particle size can be determined by scanning electron microscopy studies such as DLS, UV and SEM. The morphology and size of the gum Nano particles are determined by increased technique created spherical nanoparticles of size 10–280 nm. The results are given within the sort of tables and graphs. Index Terms— Guar gum, Tris sodium Trimetaphosphate, sodium hydroxide, ultrapure water, Ionic gelation method. I. INTRODUCTION Guar Gum Nano particles measures 10-1000nanometres or less. The properties of many conventional materials change when formed from nanoparticles. This is normally as a result of nanoparticles have a bigger extent per weight than larger particles that causes them to be a lot of reactive to another molecules. The size of the particle depends upon nozzle size, atomization pressure, and spray flow, body of water air temperature and quantity of cross linking.1 Drug delivery system notion is not novel in the action of some syndromes. Targeting delivery of drugs to carry a necessary dose of drug to the mark, proper carriers of drug were required. These Nano particle carriers have key potential application for the admin of health-giving Manuscript revised June 4, 2019 and published on July 10, 2019 Mr.G.Muthaih, Department of Chemistry, Acharya Nagrjuna University, Guntur,Andhrapradesh,India. Mrs.S.Nagamani, Information Technology, Lakireddy balireddy college of Engineering, Mylavarm, Andhrapradesh,India. Dr.D.Ramachandran, Department of Chemistry,Acharya Nagrjuna University,Guntur,Andhra Pradesh,India. molecule. Lipase is mostly used enzyme in feed, food, pharmaceutics, which can hydrolyze obese into glycerol and full of fatty acid2, 3 . Ionic gelation (IG), also called ‗ion-induced gelation‘, ends up in small particles (MPs) nanoparticles (NPs) and with defects like improper surface morphology, fragile particulate system, high dispensability index, and lack of correct surface modification sites to connect purposeful moieties.[4—6]Nanoparticles act as possible carries for numerous courses of drugs such as, antihypertensive ,agents, immunomodulators, hormones and anticancer agents.Macro molecules like proteins, nucleic acids, antibodies and peptides. [7-8] O O OH CH2OH OH OHOH HO HOO HOH2C O O HO H2C STMP Span80Glycerol Distilled Water Continious Stirring 4 Hours Nano Emulsion Kept Overnight rpm20000 Recentrifugation 30 minutes Centrifugation 30 minutes Cross linker Guargum Nano Particle rpm20000 Guargum Powder Structure of Guargum NaOH Fig 1:Systematic process of Guar gum Nano Particle preparation based on Ionic Gelation Method II. RELATED WORK Nano Particles are a category of materials with diameters within the vary from 1 to 100nm. These systems area unit created unremarkably in nature, and that they area unit referred to as colloids, aerosols and submicron solids; these area unit dirt particles and suspended solids in liquid systems, smoke, clouds and mist. Different nanoparticles area unit deliberately created for distinctive applications in areas of medication and physics[9-11].Fabricated metal colloids are used for the so many years in manufacturing of glass[12-14]. PCA ways applied with numerous qualitative analysis techniques have mature to become themedicine analysis, as well as techniques capable of aiding within the diagnosis of multiple diseases like breast and cervical cancer[17,18] and leukemia [19]. GGNPs has been widly used for breast cancer delivery to the drug unless retarding property and condition Preparation and characterization of Guar gum Nano Particle through DLS, UV and SEM Gunti Muthaiah, S.Nagamani, Dr.D.Ramachandran
  • 2. International Journal of Research in Advent Technology, Vol.7, No.6, June 2019 E-ISSN: 2321-9637 Available online at www.ijrat.org 45doi: 10.32622/ijrat.76201928 to microorganism degradation within the intensive. Very little data is out there within the open literature for the chance of exploitation gum based mostly Nano sized materials as a drug carrier In this an attempt is formed in getting ready Nano sized uncoated and catalyst functionalized gum NPs by ionic gelation and cross-linking methodology. Particle size poly dispersity index, and size was established by DLS, UV, and SEM. III.EXPERIMENTAL A .Chemicals required Guargum(Mw220kDa),Ttrisodium trimetaphosphate,Na3P3O9 (STMP), and sodium hydroxide (NaOH).All solutions were ready with ultrapure water. B. Preparation Preparation of cross-linked nanoparticles varied amounts of GG (concentration starting from 0.05 to 0.2 % w/v) were additional in to a 2M NaOH solution (100 ml, pH=12.0) and were allowed to hydrate for a minimum of 2h underneath constant magnetic stirring at temperature.A STMP solution (100mL, concentration varied from 0.2 to 10% w/v) was then additional at a rate of flow of one mL/min employing a peristaltic pump, and therefore the reaction mixture was then ceaselessly stirred nightlong. The resultant mixture dispersion was dialyzed against H2O till neutral pH (approx.72h). An aliquot of the sample suspension was unbroken for particle size measurements, whereas the remaining product was freeze-dried by freeze drying then keep in an exceedingly desiccator. Solvent Polymer in aqueous phase (Guar gum) O/W Emulsion Nano Emulsion Cross linked Nano particles in preparative media Cross linked Nano particles in preparative media Sonication Span80 (Emulsifier) Glycerol NaoH STMP (Cross linker) Tri sodium trimetaphasphate Centrifugation After that again Wash and Centrifugation Stirring one Complete Night Fig 2: Schematic representation of nano particle preparation Batch GG concentrati on (%) STMP concentrati on (%) Size SDn m PD I GGNP 0.5 10 780±1.4 0.5 1 GGNP 2 0.5 5 460±1.3 0.4 GGNP 3 0.5 2.5 417±1.2 0.3 2 GGNP 4 0.4 1 360±1.6 0.2 8 GGNP 5 0.4 0.5 537±8.9 0.2 5 GGNP 6 0.4 0.25 450±12.4 0.2 GGNP 7 0.3 0.05 387±0.6 0.1 8 GGNP 8 0.3 0.03 593±1.3 0.1 2 GGNP 9 0.3 0.02 208±0.9 0.1 1 Table 1: Characterization of different Nanoparticle Fig 3: STMP Concentration and PDI C. DLS Analysis Particle size and DLS measurements the common hydraulics diameter of the nanoparticles determined in water at 25 °C by dynamic lightweight scattering measurements employing a Malvern Zeta size ZS90 (Malvern Instruments, Worcester, UK). The same Instrument allow the determination of 3 measurements and polydispersity index (PDI). Additionally, period of time dynamic nanoparticle image was achieved by nanoparticle following analysis (NTA) employing a Nano sight LM10 instrument prepared with a sample chamber with a 532nm optical maser and a 560 nm long pass filter. The particle size was calculated exploitation the Stokes–Einstein 0 0.1 0.2 0.3 0.4 0.5 0.6 10.00 2.50 0.50 0.05 0.02 PDI % Concentration
  • 3. International Journal of Research in Advent Technology, Vol.7, No.6, June 2019 E-ISSN: 2321-9637 Available online at www.ijrat.org 46doi: 10.32622/ijrat.76201928 Fig. 4: (b) Guar gum Nano particle Correlation function D. UV-Vis Spectra Analysis: The reduction of pure guar gum Nano particles was monitored under UV–vis spectrophotometer (Thermo scientific-Genesys10S) 3ml of sample was withdrawn .The absorbance was measured. UV-vis spectral analysis was done by between 300-700nm.Guar gum nanoparticles formation and the stability of the reduced GGNPs in the filtrate were monitored by using UV-Vis Spectrophotometer (fig. 5a and 5b). An UV-Vis Spectrophotometer is one of the most important to determine the formation of polymer nanoparticles. The results were plotted and Shown in Fig.6a and 6b. The UV–Vis spectrum Showed an SPR peak of guar gum nanoparticles at 350 nm. It as well known that shape and size of the Guar gum nanoparticles reflects the absorbance peak. The absorption spectrum obtained showed a strong surface Plasmon resonance band maximum at 355 nm (fig. 5) a characteristic peak of guar gum nanoparticles. Fig 5: (a) Guar gum with solvent (b) after addition of cross linker STMP Fig.6 (a): UV-Visible spectral analysis of synthesized guar gum nano particles without cross linker Fig.6 (b): UV-Visible spectral analysis of synthesized guar gum nanoparticles with cross linker (STMP) E. SEM ANALYSIS The scanning microscope (SEM) is one of the foremost versatile instruments on the market for the check and analysis of the microstructure morphology and chemical conformation characterizations. SURAFCE MORPHOLOGY The surface morphology of nanoparticles was studied by scanning microscopy employing a(SEM Jeol JSM-6060LV) Instrument. Sample were placed on stumps, dehydrated with chemical element Associate in Nursing covered with golden alloy in a chemical element atmosphere (current 20 mA, pressure 10e-3 Pa (employing a coater (Quorum, Q 150RES)).
  • 4. International Journal of Research in Advent Technology, Vol.7, No.6, June 2019 E-ISSN: 2321-9637 Available online at www.ijrat.org 47doi: 10.32622/ijrat.76201928 Fig.7(a) SEM Micrograph of 100nm Fig 7(b) SEM micrograph of Guar gum Nano Particles. Fig. 7(c) SEM Micrograph of 1µm Fig.7(d) Guar gum particles V.RESULT AND DISCUSSION The scanning electron microscope (SEM) is one among the foremost versatile instruments on the market for the investigation and analysis of the microstructure morphology and chemical conformation characterization. Guar gum Nano particles were investigated by SEM as show Fig-7(a, b) The SEM micrographs the particle size were obtained 10-100 nm which is show in the Fig 7(a, b c d). VI.CONCLUSION The techniques namely DLS, UV and SEM mainly used for morphological studies of nanoparticles. Various researchers used these techniques to point out that the made Nano particles were additional or less uniform in size and form. However, challenges and also the success for the researchers during this rising field would rely to an oversized extent on the provision, value and simple handling and performance of the delicate techniques delineate during this paper. Further, the standard and extent of data derived through these techniques i.e. DLS, ultraviolet and SEM chemical analysis, additionally depends to an oversized extent on the extent of understanding of the user, experience and right sample preparation, characterization techniques for nanoparticle employed in drug delivery application. REFERENCES [1] N.V.Ravi Kumar, Nano and Micro particles as controlled drug delivery devices,JPharma Pharmaceut Sci,2000,3(2):234-258. [2] Sunil A. Recent advances on chitosan –based macro-and nano particles in drug delivery, Journal of controlled Release 100 (2004) 5-28. [3] Ashutosh Kar, Text book of Pharmaceutical Drug analysis, ISBN (13), P293-311. [4] Patel VM, PrajapatiBG, PatelMM.Design and characterization of chitosan-containing mucoadhesive buccal patches of propranolol hydrochloride. Acta Pharms 2007 ;57:61-72. [5] Badawi AA, EI-Laithy HM, EI Qidra RK, EI Mofty H,EI dally M. Chitosan based nanocarriers for indomethacin ocular delivery. Arch Pharm Res 2008;31:1040- [6] T.Akagi, M.Higashi, T.Kaneko, T.Kida, M.Akashi, Bio macromolecules 7(2006)297-303. [7] V.P.tarchilin,pharm.RES.24(2007)1- [8] Sperling R. A., Gil P. R., Zhang F., Zanella M., Parak W., ―Biological applications of goldna nopartticles‖,J., Chem. Soc. Rev., vol.37,pp. 1896-1908,2008. [9] Weibo C., Ting G., Hao H., Jintao S., ―Applications of gold nanoparticles in cancer nanotechnology‖, Nanotechnology Science Applications, I, pp. 17-32, 2008. [10] Devika B.Ch.,Arezou A.G., Warren C.W., ―Determining the size and shape Dependence of nanoparticle -Uptake into Mammalian Cells‖,Nano Letters, vol. 6,pp. 662-668,2006.John M.T., Pure& Appl. Chem., 60,pp. 1517-1528,1988. [11] Klaus, E.; Marion, L.; Martin, M., Matthias, P.;Helmut, S., Method for manufacturing substrates with transparent and color coating stable at
  • 5. International Journal of Research in Advent Technology, Vol.7, No.6, June 2019 E-ISSN: 2321-9637 Available online at www.ijrat.org 48doi: 10.32622/ijrat.76201928 high temperature and in the presence of ultraviolet rays,U.S. Patent, 6156388,Dec. 5, 2000. [12] Jan J.G., ―On the relationships between SVD, KLT and PCA‖, pattern recognition, vol. 1-6,pp.375-381,1981. [13] Salim C., Amrane H., Boualem S., ―A new PCA-based method for data compression and enhancement of multi-frequency polarimetric SAR imagery‖,J. Intelligent data analysis, 6, pp. 187207,2002 [14] Mia H., Sanne E., ―Robust PCA and classification in biosciences. [15] Pichardo J.L., Frausto C., Barbosa o., Huerta, R., Gonzalez J.L., Ramirez C.A., Gutierrez G., Medina C., ―Ramanspectroscopy and multivariate analysis of serum sample form breast cancer patients‖, Lasers Med. Sci.,22,pp. 229-236,2007. [16] Gonzalez J.L., Rodriguez J., Martinez J.C., Frausto, C., Java L., Aguilar A., Vargas H., Martinez E., presented at Laser Florence 2009, International Congress Laser Medicine with pre conference Courses, November 6-November 7, Springer, Florence 2009,12(26):pp. 91-95. [17] Martinez J.C., Gonzalez J.L., Frausto C., Miranda M.L., Soria C., Medina J., presented at Laser Florence 2008, International Congress Laser medicine with Pre conference Courses. AUTHOR PROFILE Mr.Gunti Muthaiah Research scholar in department of Chemistry at Acharya Nagarjuna University, Guntur. He published 4 International Journals. He attended 4 national conferences. He has 7 years of teaching experience and 5 years of Research experience. Sikhinam Nagamani. Working as an Assistant Professor in the department of IT, Lakireddy Balireddy Collge of Engineering,,Mylavarm. She attended five conferences and published 7 Interantional jornals. She has eleven years of Teaching experience.She is a member of ISTE, CSI& IAENG Dr.D.Ramachandran working as associate professor in Department of chemistry at Acharya Nagarjuna University,Guntur. He published 38 national journals and 68 International journals. He attended 40 national conferences and 6 International Conferences.