SlideShare a Scribd company logo
1 of 11
Download to read offline
IJOPILS. MAR 2015; 3(4):9-19
Vol: 3(4) March 2015
9
www.ijopils.com
International Journal of Pharmacy and Integrated Life Sciences
“Where improvisation meets innovation”
www.ijopils.com
REVIEW ARTICLE ISSN: 2320 - 0782 V3-(I4) PG(9-19)
Role of Nanotechnology in Cosmetics
Aakriti Kapoor1
, Pratibha Nand*1
1. Maharaja Surajmal Institute of Pharmacy, New Delhi, India.
ABSTRACT
The cosmetic industry is steadily probing for discovery of new formulations with effective delivery
system having biological activity. Nanoscience is one of the widely used technologies and finds
its applications in the cosmetic industry. Nanotechnology thus is a transformative and new
technical revolution and is being used for alteration of physical properties of an enormous range
of products from moisturisers, sun blocks, anti-ageing lotions to liquid make up, hair styling and
colouring agents, soothing creams etc. However the use of various techniques such as the
liposome, niosome, nanocrystals, microemulsion, nanoemulsion, nanosome, nanotubes have their
own share of advantages and disadvantages. This article aims at describing some of the
nanotechnologies used in the cosmetic industry.
KEYWORDS : Cosmetics, liposome, niosomes, nanoemulsions, anti-ageing and sun blocks.
Article received on: 11/03/2015 Article accepted on: 28/03/2015
Corresponding Author: Dr. Pratibha Nand
Address : Maharaja Surajmal Institute of Pharmacy, New Delhi, India
Email : pratibha.msip@gmail.com
Nand et. Al. , Volume 3 – Issue 4
Vol: 3(4) March 2015
10
www.ijopils.com
INTRODUCTION
Nanotechnology is most often described as the manufacture and manipulation of purpose-made
structures which are at least smaller than 100nm. The US FDA defines cosmetics, as “articles
intended to be rubbed, poured, sprinkled, or sprayed on, introduced into, or otherwise applied to
the human body for cleansing, beautifying, promoting attractiveness, or altering the appearance;
and articles intended for use as a component of any such articles except that such term shall not
include soap1
[FD&C Act, sec. 201]. Cosmetics account to be a paramount constituent of one’s
routine life, ranging from the use of moisturisers to toothpastes to perfumes to beauty products.
The European commission approximated in the year 2006 that nanoparticles are a constituent of
5% cosmetic products.2
The cosmetics industry therefore uses nano sized formulations thus
causing deeper penetration of the agents in the skin, resulting in the protection of sensitive agents,
controlled release, reduction in the amount of active molecule and additives, longer shelf life and
hence greater product effectiveness. 1, 3
Nanotechnology, a small wonder being explored by scientist in the form of nanomaterials such as
niosomes, nanocrystals, nanoemulsions, solid lipid nanoparticles (SLN), and nano structured lipid
carriers (NLC), found to give better results than the traditionally used formulations.
Nanoparticulate drug delivery system, is gaining lot of attention across biomedical, chemical foods
and cosmetics industry, because of its ability to cross the biological barriers, and get accumulated
at target site and/or improve the solubility of drugs. It has been reported solid lipid nanoparticles,
fullerenes and nanostructure lipid carriers have proved to be better safety vehicles than liposomes
because they are capable of providing enhanced skin hydration, better bioavailability and
controlled occlusion with improved stability.
Consumers using sunscreens without zinc and titanium oxide are exposed to more UVA radiation,
with increased risks of skin damage, premature aging, wrinkling, and UV-induced immune system
damage. Literature revealed the use of nanoparticles of zinc oxide and titanium dioxide in
sunscreens lotions as principal ingredients and was found to be beneficial for giving protection
against sun with decreased visibility of the white tinge which is generally observed in conventional
compositions.
Nand et. Al. , Volume 3 – Issue 4
Vol: 3(4) March 2015
11
www.ijopils.com
The present review explores the current state of knowledge on nanotechnology in cosmetics,
various potential risks involved to human beings and the measures taken to ensure the development
of safe and effective nano-based products in cosmetics.
1. Liposomes
Liposomes are spherical, self-closed vesicles containing phospholipid bilayer encapsulating the
core material.4
When one bilayer encapsulates the aqueous core it is called unilamellar vesicles
while in the case of many concentric bilayers are involved then multilamellar vesicles are formed.
5, 6
Liposomes are generally synthesized with self-hydrolysable lipids which allow time-controlled
release of drugs. In addition to the natural lipids, liposomes can also be made from synthetic lipids
which include non-ionic surfactant lipids and make them chemically more stable. Liposomes can
vary in size, from 15 nm up to several μm and liposomes vesicles in the range of nanometres are
called nanoliposomes.2
Recently, a new type of liposomes called transferosomes find their
application in cosmetics as they are more elastic than liposomes. 7
Transferosomes size varies in
the range of 200-300 nm and can penetrate the skin with improved efficiency than liposomes.
Liposomes are actually nano scale lipid based vehicles. Micelles and polymerosomes are other
lipid based vehicles. Liposome as drug delivery systems can offer several advantages over
conventional dosage forms. These lipid based vehicles are used for increasing the solubility of
hydrophobic substances and for limiting the drug toxicity. Liposome provides sustained release
and improved penetration into tissues, especially in the case of dermal application. However,
several problems have been observed with these traditional vehicles, such as nonspecific uptake,
rapid clearance, and instability, which limit the therapeutic potential of these vehicles. Recently
certain novel preparations of these compounds have been developed to overcome these problems.
Liposomes coated with PEG, known as stealth liposome, are known to increase bioavailability
significantly because of reduced, nonspecific uptake. Liposome constructed with novel lipid
polymers have resulted in increased membrane stability.8
2. Niosomes
Nand et. Al. , Volume 3 – Issue 4
Vol: 3(4) March 2015
12
www.ijopils.com
Niosomes are non-ionic surfactant based vesicles having a structure similar to liposomes, formed
by the self-assembly of non-ionic surfactants in aqueous media. Initially developed and patented
by L’Oréal in mid past 1970’s.9
Niosome entered the market of the cosmetics offering various
advantages. “Niosome” introduced in 1987 by Lancôme.Van Hal et al. 10
and they reported that
niosome encapsulated estradiol can be delivered through the stratum corneum which is supposed
to be a protective barrier. 11, 17
Due to the high chemical stability of the surfactant as compared to
the phospholipid and no requirement of special preparation and storage conditions is an advantage
of niosomes over the liposomes, which resulted in low manufacturing costs and reduced purity
problems. 12
Use of novel surfactant (bola surfactant) for making niosomes has been found
effective for percutaneous drug delivery application. During preparation, application of heat or
agitation ensures niosomes to attain a closed bilayer structure. 13
The inner aqueous core of the
niosome could be used for delivery of the various hydrophobic and hydrophilic drugs such as
NSAIDS, anti-inflammatory, anti-infective agents and other classes of drug which offers the
biggest advantage of enhancing the transdermal drug delivery. 14, 15, 16
3. Nanoemulsions
Due to their unique properties such as their small droplet size, thermodynamic stability, efficient
drug delivery system, desirable sensorial and aesthetic properties, the use of less surfactant,
nanoemulsions systems continued to attract a great part of cosmetic and pharmaceutical industry.18,
19
.These systems have remarkably uniform and small droplet size which results in optically
transparent or a translucent system, moreover their low viscosity leads to good spreadability.
Problems associated with the conventional emulsion systems are like creaming, flocculation,
sedimentation and coalescence which are not observed with nanoemulsions, making them more
acceptable in the cosmetic industry. These systems constitute an effective transport system due to
their increased free energy and high surface area. 20
Nanoemulsions may be water in oil, oil in
water or a bi-continuous one along with a suitable combination of surfactants or co-surfactants,
which is approved for human consumption (GRAS).21
Nanoemulsions are a better choice for
transport of lipophilic substances as compared to liposome due to their lipophilic interior and
moreover their effective delivery of drug make them popular in the industry. 20
Nand et. Al. , Volume 3 – Issue 4
Vol: 3(4) March 2015
13
www.ijopils.com
4. Microemulsions
In order to overcome the shortcomings of the prevalent formulations such as thermodynamic
instability and limited shelf life, the microemulsions was introduced by Hoar and Schulman in
1943 as potential delivery system. These transparent, isotropic, monophasic systems have
distinctive properties like large interfacial area, ultralow interfacial tension, thermodynamic
stability, dynamic microstructure , long shelf life, low viscosity , ability to solubilise immiscible
liquids and with reasonably lower cost of production when compared to the conventional
formulations.18-22, 24
As these systems can consume high amount of lipophilic constituents in the inner oil phase, which
is essential component of formulation as it increases their usefulness. Presence of nonpolar, polar
and interfacial realm allows enveloping constituents of varying range of solubility.22, 23
Their small
droplet size, density and increased surface area makes the droplets clinch with the skin resulting
in increased permeation. 24
Microemulsions as skin care product contain tetraethylene glycol monododecyl ether, sodium
alkyl sulphate, lecithin, alkyl dimethyl amine oxide, propranolol, hexadecane, isopropyl myristate
as their constituents25
. Hair care products also contain amino functional poly organosiloxane and
acid or metal salt.
5. Nanocrystals
Nanocrystals are clusters of hundreds to tens of thousands of atoms and their size ranges between
10 to 400 nm. The properties of nanocrystals like band gap, charge conductivity, and melting point
are dependent on their size and surface area. Nanocrystals have generally been used in the
pharmaceutical industry to overcome problems such as poor solubility, low bioavailability and
problems with delivery of drugs.26
Nanocrystals are beneficial for the pharmaceutical industry due
to their enhanced dissolution velocity, saturation solubility and reproducibility of oral absorption,
improved dose bioavailability and increased patient compliance by reducing number of doses.27
The first cosmetic product that appeared in market Juvena in 2007 and La Prairie in 2008 which
consisted of two poorly soluble plant antioxidants rutin and hespiridine that previously could not
be used for dermal purpose, once formulated as nanocrystals they had became available dermally
as per the measured antioxidant effect .2
The first nanocrystals product Rapamune® (rapamycin,
Nand et. Al. , Volume 3 – Issue 4
Vol: 3(4) March 2015
14
www.ijopils.com
immunosuppressive) was placed on market in year 2000 by Wyeth.26
In 2001, the second product
Emend® was introduced by the company Merck (aprepitant capsule, antiemetic), which had a
much higher nano crystal loading when compared to Rapamune.28
Nanocrystals generally reduce
the dose to be administered and provide a sustained release effect with better patient compliance.2
For their commercial production, pearl milling and high pressure homogenisation can be used
which is also accepted by regulatory authorities. The first four marketed products containing
nanocrystals such as Rapamune®, Emend®, Tricor® and Megace ES® were prepared by Pearl
mill technology by Elannanosystems. 28, 29
6. Dendrimers
The term dendrimer has been derived from two Greek words “Dendron” meaning tree and “Meros”
meaning part.30- 32
The chemistry of dendrimers was introduced by Fritz Vogtle and co-workers in
1978.30
The dendrimers are three-dimensional, hyper-branched, globular, monodisperse synthetic
polymers having well defined shape, molecular weight and size.33
A dendrimer essentially
comprises of a central core with branches that are radically attached to the central core 33
and
terminal functional group attached to outer series of branches.34
A wide variety of dendrimers are
available depending upon the compatibility and other properties. Dendrimers can be prepared by
Divergent, Convergent, and Double exponential or mixed methods. 35
Dendrimers have an
important contribution in the cosmetic industry, brands such as L’Oreal and Unilever have patents
in using dendrimer for the production of mascara, nail polish and sprays, gels and lotions
respectively.36-37
Besides these dendrimers have wide variety of applications ranging from
therapeutic, diagnostic to pharmaceutical industry.
SAFETY CONCERNS
One of the most popular questions raised in the media and peer-reviewed articles is “how safe is
nanotechnology38
. It has been established that nano sized particles are present in sunscreens and
cosmetics and they have raised the issue of safety regarding the dermal penetration of these
particles, leading to ill health. Penetration and dermal exposure are important issues when handling
engineered nanomaterials. Zinc oxide and titanium dioxide are being used as an effective Ultra-
violet blocking agent in sunscreen lotions.39
The point is when these engineered nanomaterials
Nand et. Al. , Volume 3 – Issue 4
Vol: 3(4) March 2015
15
www.ijopils.com
come in contact with human skin and penetrate through the layers of skin what impact they have
on skin. Tinkle et al reported that latex particles of size smaller than one micrometer penetrate
outer layers of skin during flexing. Some studies show that presence of healthy intact skin acts as
a good barrier against nano structured particles 40
. Ryman Rasmussen et al have reported that
quantum dots of different size, shape with coating can penetrate through outer layers of pig skin
and enter the epidermis and dermis in 24 hours, the smallest particles (4.6 nm in diameter) had
shown localisation in the epidermis and the dermis within period of 8 hours irrespective of the
coating material and larger non spherical particles showed a penetration rate dependent on the
coating.40
CONCLUSION
As nanotechnology moves toward widespread commercialization and it is a transformative
technology which is merging with information technology, biology and social science. It is
expected to reinvigorate discoveries and innovations in many areas of the economy. Nanomedicine
is dominated by nanoparticulate drug delivery systems because of their ability to cross biological
barriers.
Nand et. Al. , Volume 3 – Issue 4
Vol: 3(4) March 2015
16
www.ijopils.com
REFERENCES
1. Adnan A, Mohammad R, Farhan JA, Zeenat IK, Roop KK, Mohammed A and Sushama T.
Emerging role of microemulsions in cosmetics ; Recent Patents on Drug Delivery &
Formulation. 2008; 2: 275-289.
2. Anju S,Senthil KM, Mahadevan N. Nanotechnology: a promising approach for cosmetics;
International Journal of Recent Advances in Pharmaceutical Research. 2012; 2(2): 54-61.
3. Sabine G, André G, Myrtill S, Ulrich F, Michael N. Nanotechnology in cosmetics. Nano
trust Dossier No.008n. 2010.
4. Bangham, AD and Horne RW. Negative staining of phospholipids and their structured
modofication by surface active agents as observed in the electron microscope. J Mol Biol.
1964; 8: 660–668.
5. Papahadjopoulos D. Liposomes and their use in biology and medicine. NY Acad Sci 1978;
1–412.
6. Lasic DD. Applications of liposomes , Liposome Technology, Inc. 1050 Hamilton
Court,Menlo Park, California, USA 94025
7. Cevc G. Transferosomes, liposomes and other lipid suspensions on the skin: permeation
enhancement, vesicle penetration, and transdermal drug delivery. Crit Rev Ther Drug
Career Syst. 1996; 13: 257–388,
8. Thong HY, Zhai H, Maibach HI. Percutaneous penetration enhancers: An overview. Skin
Pharmacol Physiol. 2007; 20, 272–282.
9. Procédé de fabrication de dispersions aqueuses de spérules lipidiques et nouvelles
compositions correspondantes, L’Oréal, French Patent 2315991, 1975.
10. Cosmetic and pharmaceutical compositions containing niosomes and a water-soluble
polyamide, and a process for preparing these compositions, L’Oréal, US Patent 4830857,
1989.
11. Van H D, Vanrensen A, Devringer T, Junginger H, Bouwstra J, Diffusion of estradiol from
non-ionic surfactant vesicles through human stratum-corneum in-vitro. STP Pharm Sci.
1996; 6: 72–78.
Nand et. Al. , Volume 3 – Issue 4
Vol: 3(4) March 2015
17
www.ijopils.com
12. Pushpendra KT, Choudary S, Ankur S, Devindera PS, Vikas C. Niosomes: study on noval
drug delivery system-A review. International Journal of Pharmaceutical and Research and
Development. 2012; 3: 100-106.
13. Paolino D, Muzzalupo R, Ricciardi A, Celia C, Picci N, Fresta M. In vitro and in vivo
evaluation of Bola-surfactant containing niosomes for transdermal delivery. Biomed
Microdevices. 2007;9: 421–433.
14. Uchegbua IF, Vyas SP. Non-ionic surfactant based vesicles (niosomes) in drug delivery.
International Journal of Pharmaceutics. 1998;172: 1-2, 33-70.
15. Reddy DN, Udupa N. Formulation and evaluation of oral and transdermal preparations of
flurbiprofen and piroxicam incorporated with different carriers. Drug Dev Ind Pharm.
1993; 19: 843–852.
16. Walker W, Brewer JM, Alexander J. Lipid vesicle-entrapped influenza A antigen
modulates the influenza A specific human antibody response in immune reconstituted
SCID-human mice. Eur J Immunol. 1996; 26: 1664–1667,
17. Anuradha P, Vandana P. Novel lipid based systems for improved topical delivery of
antioxidants. Household and Personal Care today. 2009; 4: 5-8.
18. Amnon C, Sintov and Haim V, Leavy. A microemulsion based delivery system for the
delivery of therapeutics. Innovation in Pharmaceutical Technology.2007; 23: 68-72.
19. Danielsson I, Lindman B. The definition of microemulsion. Colloid Surf 1981; 3: 391-392.
20. Narang AS, Delmarre D, Gao D. Stable drug encapsulation in micelles and
microemulsions. Int J Pharm. 2007; 345: 9-25.
21. Yuan Y, Li SM, Mo FK, Zhong DF. Investigation of microemulsion system for transdermal
delivery of meloxicam. Int J Pharm. 2006; 321: 117-123.
22. Kreilgaard M, Pedersen EJ, Jaroszewski JW. NMR characterization and transdermal drug
delivery potential microemulsion systems. J Control Release. 2000; 69: 421-433.
23. Kreilgaard M. Influence of microemulsion on cutaneous drug delivery. Adv Drug Delivery
Rev. 2002; 54: S77-S98.
24. Elena P, Paola S, Maria RG. Transdermal permeation of apomorphine through hairless
mouse skin from microemulsions. Int J Pharm. 2001; 226: 47-51.
25. Paul BK, Moulik S. Uses and applications of microemulsions. Current Sci. 2001; 80: 25.
Nand et. Al. , Volume 3 – Issue 4
Vol: 3(4) March 2015
18
www.ijopils.com
26. Shegokar R, Muller RH.Nanocrystals: Industrially feasible multifunctional formulation
technology for poorly soluble actives. Int J Pharm. 2011; 399: 129–139.
27. Müller RH, Krause K, Mäder K. Method for controlled production of ultrafine
microparticles and nanoparticles. 2001b:WO/2001/003670
28. Petersen R. Nanocrystals for Use in Topical Cosmetic Formulations and Method of
Production Thereof. Abbott GmbH & Co., US Patent 60/866233, 2008.
29. Sanjay B, Meena B, Rachna K. Nanocrystals: Current strategies and trends. Int J Res Pharm
Biomed Sci.2012; 3: 406-419.
30. Buhleier E, Wehner W, Vogtle F. Cascade and Nonskid-chain like synthesis of molecular
cavity topologies. Synthesis. 1978; 2: 155-158.
31. Tomalia DA, Baker H, Dewald J, Hall M, Kallos G, Martin S, Roeck J, Ryder J, Smith P.
A new class of polymers: Starburst- dendritic macromolecules. Polymer Journal, 2006; 17:
117-132.
32. Newkome GR, Yao ZQ, Baker GR, Gupta VK. Cascade molecules: A new approach to
micelles, A-arborol. Journal of Organic Chemistry. 1985; 50: 2003-2006.
33. Cheng Y, Tongwen X. Dendrimers as potential drug carriers. Part I. Solubilisation of non-
steroidal anti-Inflammatory drugs in the presence of polyamidoamine dendrimers. Eur J
Med Chem. 2005; 40: 1188-1192.
34. Caminade AM, Laurent R, Majoral JP. Characterization of dendrimers. Advanced Drug
Deliv Rev. 2005; 57: 2130-2146.
35. Sonke S, Tomalia DA. Dendrimers in biomedical application reflection on the field.
Advanced Drug Deliv Rev. 2005; 57: 2106-2129.
36. Jean M, Sylvie G. Use of hyper branched polymer and dendrimers comprising a particular
group as film- forming agent, film forming composition comprising same and use
particularly in cosmetics and pharmaceutics, L’Oreal, U S Patent 6432423, 2002.
37. Delphine A, Serge F. Self- tanning cosmetic composition, L’Oreal, U.S Patent 6399048,
2002.
38. Hood E. Environ. Nanotechnology: looking as we leap. Environmental Health Perspectives
Health Perspect. 2004; 112 (13): A741-A749
Nand et. Al. , Volume 3 – Issue 4
Vol: 3(4) March 2015
19
www.ijopils.com
39. Popov A P, Priezzhev AV, Lademann J, R Myllyla. TiO2 nanoparticles as an effective UV-
B radiation skin-protective compound in sunscreens. J Phys D Appl Phys 2005; 38 (15):
2564-2570.
40. Willander M, Omer N, Lozovik YE, Al-Hilli SE, Chiragwandi Z, QH Hu, Zhao QX,
Klason P. Solid and soft nanostructured materials: Fundamentals and applications
. Microelectron J. 2005; 36 (11): 940-949.

More Related Content

What's hot

Nanoparticles powerpoint
Nanoparticles powerpointNanoparticles powerpoint
Nanoparticles powerpointeyfanatic
 
Nano drug delivery
Nano drug deliveryNano drug delivery
Nano drug deliverytabirsir
 
Polymeric nanoparticles A Novel Approach
Polymeric nanoparticles  A Novel ApproachPolymeric nanoparticles  A Novel Approach
Polymeric nanoparticles A Novel Approachshivamthakore
 
Nanoparticles for Cancer Therapy
Nanoparticles for Cancer TherapyNanoparticles for Cancer Therapy
Nanoparticles for Cancer TherapyNimra Iqbal
 
Biotechnology in Product Development
Biotechnology in Product DevelopmentBiotechnology in Product Development
Biotechnology in Product DevelopmentJanine Samelo
 
Nanotechnology In Bio Medical Applications
Nanotechnology In Bio Medical ApplicationsNanotechnology In Bio Medical Applications
Nanotechnology In Bio Medical Applicationslusik
 
Phytosynthesis metal nanoparticle
Phytosynthesis metal nanoparticlePhytosynthesis metal nanoparticle
Phytosynthesis metal nanoparticlearchana achu
 
New microsoft office power point presentation 111
New microsoft office power point presentation 111New microsoft office power point presentation 111
New microsoft office power point presentation 111Deepak Upadhyay
 
NANOTECHNOLOGY FOR CANCER THERAPY RECENT DEVELOPMENTS
NANOTECHNOLOGY FOR CANCER THERAPY RECENT DEVELOPMENTSNANOTECHNOLOGY FOR CANCER THERAPY RECENT DEVELOPMENTS
NANOTECHNOLOGY FOR CANCER THERAPY RECENT DEVELOPMENTSroshan telrandhe
 
Introduction of Nanotechnology
Introduction of Nanotechnology Introduction of Nanotechnology
Introduction of Nanotechnology NIKET SURESH POWAR
 
Applications of nanotechnology in pharmacy
Applications of nanotechnology in pharmacyApplications of nanotechnology in pharmacy
Applications of nanotechnology in pharmacySaravanan subramaniyam
 
Application of Nanoparticles
Application of NanoparticlesApplication of Nanoparticles
Application of NanoparticlesLAKSHMI NARAYAN
 
Application of nanoparticals in drug delivery system
Application of nanoparticals in drug delivery systemApplication of nanoparticals in drug delivery system
Application of nanoparticals in drug delivery systemMalay Jivani
 
Use of Nanotechnology in Diagnosis and Treatment of Cancer
Use of Nanotechnology in Diagnosis and Treatment of CancerUse of Nanotechnology in Diagnosis and Treatment of Cancer
Use of Nanotechnology in Diagnosis and Treatment of CancerAnas Indabawa
 

What's hot (20)

Nanoparticles powerpoint
Nanoparticles powerpointNanoparticles powerpoint
Nanoparticles powerpoint
 
Nano drug delivery
Nano drug deliveryNano drug delivery
Nano drug delivery
 
Polymeric nanoparticles A Novel Approach
Polymeric nanoparticles  A Novel ApproachPolymeric nanoparticles  A Novel Approach
Polymeric nanoparticles A Novel Approach
 
Nanoparticles for Cancer Therapy
Nanoparticles for Cancer TherapyNanoparticles for Cancer Therapy
Nanoparticles for Cancer Therapy
 
Biotechnology in Product Development
Biotechnology in Product DevelopmentBiotechnology in Product Development
Biotechnology in Product Development
 
Nanotechnology In Bio Medical Applications
Nanotechnology In Bio Medical ApplicationsNanotechnology In Bio Medical Applications
Nanotechnology In Bio Medical Applications
 
Phytosynthesis metal nanoparticle
Phytosynthesis metal nanoparticlePhytosynthesis metal nanoparticle
Phytosynthesis metal nanoparticle
 
Nano Fiber
Nano FiberNano Fiber
Nano Fiber
 
New microsoft office power point presentation 111
New microsoft office power point presentation 111New microsoft office power point presentation 111
New microsoft office power point presentation 111
 
Nanogel
NanogelNanogel
Nanogel
 
NANOTECHNOLOGY FOR CANCER THERAPY RECENT DEVELOPMENTS
NANOTECHNOLOGY FOR CANCER THERAPY RECENT DEVELOPMENTSNANOTECHNOLOGY FOR CANCER THERAPY RECENT DEVELOPMENTS
NANOTECHNOLOGY FOR CANCER THERAPY RECENT DEVELOPMENTS
 
Introduction of Nanotechnology
Introduction of Nanotechnology Introduction of Nanotechnology
Introduction of Nanotechnology
 
Nanopolymer
NanopolymerNanopolymer
Nanopolymer
 
Applications of nanotechnology in pharmacy
Applications of nanotechnology in pharmacyApplications of nanotechnology in pharmacy
Applications of nanotechnology in pharmacy
 
Nanoemulsions
NanoemulsionsNanoemulsions
Nanoemulsions
 
Application of Nanoparticles
Application of NanoparticlesApplication of Nanoparticles
Application of Nanoparticles
 
Application of nanoparticals in drug delivery system
Application of nanoparticals in drug delivery systemApplication of nanoparticals in drug delivery system
Application of nanoparticals in drug delivery system
 
Nanoemulsion
NanoemulsionNanoemulsion
Nanoemulsion
 
Use of Nanotechnology in Diagnosis and Treatment of Cancer
Use of Nanotechnology in Diagnosis and Treatment of CancerUse of Nanotechnology in Diagnosis and Treatment of Cancer
Use of Nanotechnology in Diagnosis and Treatment of Cancer
 
Nanobiotechnology
NanobiotechnologyNanobiotechnology
Nanobiotechnology
 

Viewers also liked

Nanoparticles in Sunscreens & Cosmetics
Nanoparticles in Sunscreens & Cosmetics Nanoparticles in Sunscreens & Cosmetics
Nanoparticles in Sunscreens & Cosmetics v2zq
 
recent updates in cosmetic technology
recent updates in cosmetic technologyrecent updates in cosmetic technology
recent updates in cosmetic technologyKhaled Al-Qaoud
 
Solid lipid nanoparticles
Solid lipid nanoparticlesSolid lipid nanoparticles
Solid lipid nanoparticlesAnay Kacharia
 
Vesicular drug delivery system
Vesicular drug delivery systemVesicular drug delivery system
Vesicular drug delivery systemVijaykumar Chavan
 
Physicochemical Properties effect on Absorption of Drugs
Physicochemical Properties effect on Absorption of DrugsPhysicochemical Properties effect on Absorption of Drugs
Physicochemical Properties effect on Absorption of DrugsSuraj Choudhary
 
Solubility (Physical Pharmacy)
Solubility (Physical Pharmacy)Solubility (Physical Pharmacy)
Solubility (Physical Pharmacy)Areej Abu Hanieh
 
Hype vs. Reality: The AI Explainer
Hype vs. Reality: The AI ExplainerHype vs. Reality: The AI Explainer
Hype vs. Reality: The AI ExplainerLuminary Labs
 
3 Things Every Sales Team Needs to Be Thinking About in 2017
3 Things Every Sales Team Needs to Be Thinking About in 20173 Things Every Sales Team Needs to Be Thinking About in 2017
3 Things Every Sales Team Needs to Be Thinking About in 2017Drift
 

Viewers also liked (11)

Nanoparticles in Sunscreens & Cosmetics
Nanoparticles in Sunscreens & Cosmetics Nanoparticles in Sunscreens & Cosmetics
Nanoparticles in Sunscreens & Cosmetics
 
Nanotechnology in nutraceuticals and cosmetics
Nanotechnology in nutraceuticals and cosmeticsNanotechnology in nutraceuticals and cosmetics
Nanotechnology in nutraceuticals and cosmetics
 
recent updates in cosmetic technology
recent updates in cosmetic technologyrecent updates in cosmetic technology
recent updates in cosmetic technology
 
Programming in c++
Programming in c++Programming in c++
Programming in c++
 
Solid lipid nanoparticles
Solid lipid nanoparticlesSolid lipid nanoparticles
Solid lipid nanoparticles
 
Vesicular drug delivery system
Vesicular drug delivery systemVesicular drug delivery system
Vesicular drug delivery system
 
Physicochemical Properties effect on Absorption of Drugs
Physicochemical Properties effect on Absorption of DrugsPhysicochemical Properties effect on Absorption of Drugs
Physicochemical Properties effect on Absorption of Drugs
 
Solubility (Physical Pharmacy)
Solubility (Physical Pharmacy)Solubility (Physical Pharmacy)
Solubility (Physical Pharmacy)
 
Nanotechnology ppt
Nanotechnology pptNanotechnology ppt
Nanotechnology ppt
 
Hype vs. Reality: The AI Explainer
Hype vs. Reality: The AI ExplainerHype vs. Reality: The AI Explainer
Hype vs. Reality: The AI Explainer
 
3 Things Every Sales Team Needs to Be Thinking About in 2017
3 Things Every Sales Team Needs to Be Thinking About in 20173 Things Every Sales Team Needs to Be Thinking About in 2017
3 Things Every Sales Team Needs to Be Thinking About in 2017
 

Similar to role of nanotechnology in cosmetics

Influence of nanotechnology in cosmetology
Influence of nanotechnology in cosmetologyInfluence of nanotechnology in cosmetology
Influence of nanotechnology in cosmetologyDr. sreeremya S
 
Advances_of_Non-Ionic_Surfactant_Vesicles_Niosomes.pdf
Advances_of_Non-Ionic_Surfactant_Vesicles_Niosomes.pdfAdvances_of_Non-Ionic_Surfactant_Vesicles_Niosomes.pdf
Advances_of_Non-Ionic_Surfactant_Vesicles_Niosomes.pdftabindakiran20feb
 
Nano-niosomes in drug, vaccine and gene delivery: a rapid overview
Nano-niosomes in drug, vaccine and gene delivery: a rapid overviewNano-niosomes in drug, vaccine and gene delivery: a rapid overview
Nano-niosomes in drug, vaccine and gene delivery: a rapid overviewNanomedicine Journal (NMJ)
 
Novel approaches to parenteral drug delivery system
Novel approaches to parenteral drug delivery systemNovel approaches to parenteral drug delivery system
Novel approaches to parenteral drug delivery systemKarrolla Shiny
 
Solid lipid nanoparticles ppt
Solid lipid nanoparticles pptSolid lipid nanoparticles ppt
Solid lipid nanoparticles pptPriyansha Singh
 
Nanosponge Leveraging Novel Technology
Nanosponge Leveraging Novel TechnologyNanosponge Leveraging Novel Technology
Nanosponge Leveraging Novel Technologyijtsrd
 
19. nanotechnology book chapter.pdf
19. nanotechnology book chapter.pdf19. nanotechnology book chapter.pdf
19. nanotechnology book chapter.pdfRAJESHKUMAR428748
 
NANOTECHNOLOGY IN DEVELOPMENT OF DRUG DELIVERY SYSTEM
NANOTECHNOLOGY IN DEVELOPMENT OF DRUG DELIVERY SYSTEMNANOTECHNOLOGY IN DEVELOPMENT OF DRUG DELIVERY SYSTEM
NANOTECHNOLOGY IN DEVELOPMENT OF DRUG DELIVERY SYSTEMMakrani Shaharukh
 
Application of nanotechnology in dairy industry
Application of nanotechnology in dairy industryApplication of nanotechnology in dairy industry
Application of nanotechnology in dairy industryChiragPrajapati70
 
Application of Nanotechnology in Dairy Industry.pptx
Application of Nanotechnology in Dairy Industry.pptxApplication of Nanotechnology in Dairy Industry.pptx
Application of Nanotechnology in Dairy Industry.pptxChirag Prajapati
 
Microspheres and microcapsules
Microspheres and microcapsulesMicrospheres and microcapsules
Microspheres and microcapsulesJayBhavsar41
 
Nanoemulsion : A versatile drug delivery system
Nanoemulsion : A versatile drug delivery systemNanoemulsion : A versatile drug delivery system
Nanoemulsion : A versatile drug delivery systemDeeptiMSati
 
Niosomes: An excellent tool for drug delivery
Niosomes: An excellent tool for drug deliveryNiosomes: An excellent tool for drug delivery
Niosomes: An excellent tool for drug deliverypharmaindexing
 
Neha (m pharm) nanoparticle
Neha (m pharm) nanoparticleNeha (m pharm) nanoparticle
Neha (m pharm) nanoparticleHemant Rawat
 
liposomes and nanoparticles drug delivery system
liposomes and nanoparticles drug delivery systemliposomes and nanoparticles drug delivery system
liposomes and nanoparticles drug delivery systemShreyaBhatt23
 

Similar to role of nanotechnology in cosmetics (20)

Influence of nanotechnology in cosmetology
Influence of nanotechnology in cosmetologyInfluence of nanotechnology in cosmetology
Influence of nanotechnology in cosmetology
 
Advances_of_Non-Ionic_Surfactant_Vesicles_Niosomes.pdf
Advances_of_Non-Ionic_Surfactant_Vesicles_Niosomes.pdfAdvances_of_Non-Ionic_Surfactant_Vesicles_Niosomes.pdf
Advances_of_Non-Ionic_Surfactant_Vesicles_Niosomes.pdf
 
Jddr 190
Jddr 190Jddr 190
Jddr 190
 
A 1
A 1A 1
A 1
 
Nano-niosomes in drug, vaccine and gene delivery: a rapid overview
Nano-niosomes in drug, vaccine and gene delivery: a rapid overviewNano-niosomes in drug, vaccine and gene delivery: a rapid overview
Nano-niosomes in drug, vaccine and gene delivery: a rapid overview
 
Novel approaches to parenteral drug delivery system
Novel approaches to parenteral drug delivery systemNovel approaches to parenteral drug delivery system
Novel approaches to parenteral drug delivery system
 
Hndds (cognosy)
Hndds (cognosy)Hndds (cognosy)
Hndds (cognosy)
 
Solid lipid nanoparticles ppt
Solid lipid nanoparticles pptSolid lipid nanoparticles ppt
Solid lipid nanoparticles ppt
 
Nanosponge Leveraging Novel Technology
Nanosponge Leveraging Novel TechnologyNanosponge Leveraging Novel Technology
Nanosponge Leveraging Novel Technology
 
What is nanotec-W.pptx
What is nanotec-W.pptxWhat is nanotec-W.pptx
What is nanotec-W.pptx
 
19. nanotechnology book chapter.pdf
19. nanotechnology book chapter.pdf19. nanotechnology book chapter.pdf
19. nanotechnology book chapter.pdf
 
NANOTECHNOLOGY IN DEVELOPMENT OF DRUG DELIVERY SYSTEM
NANOTECHNOLOGY IN DEVELOPMENT OF DRUG DELIVERY SYSTEMNANOTECHNOLOGY IN DEVELOPMENT OF DRUG DELIVERY SYSTEM
NANOTECHNOLOGY IN DEVELOPMENT OF DRUG DELIVERY SYSTEM
 
Application of nanotechnology in dairy industry
Application of nanotechnology in dairy industryApplication of nanotechnology in dairy industry
Application of nanotechnology in dairy industry
 
Application of Nanotechnology in Dairy Industry.pptx
Application of Nanotechnology in Dairy Industry.pptxApplication of Nanotechnology in Dairy Industry.pptx
Application of Nanotechnology in Dairy Industry.pptx
 
Microspheres and microcapsules
Microspheres and microcapsulesMicrospheres and microcapsules
Microspheres and microcapsules
 
Nanoemulsion : A versatile drug delivery system
Nanoemulsion : A versatile drug delivery systemNanoemulsion : A versatile drug delivery system
Nanoemulsion : A versatile drug delivery system
 
Solid lipid nanoparticles
Solid lipid nanoparticles Solid lipid nanoparticles
Solid lipid nanoparticles
 
Niosomes: An excellent tool for drug delivery
Niosomes: An excellent tool for drug deliveryNiosomes: An excellent tool for drug delivery
Niosomes: An excellent tool for drug delivery
 
Neha (m pharm) nanoparticle
Neha (m pharm) nanoparticleNeha (m pharm) nanoparticle
Neha (m pharm) nanoparticle
 
liposomes and nanoparticles drug delivery system
liposomes and nanoparticles drug delivery systemliposomes and nanoparticles drug delivery system
liposomes and nanoparticles drug delivery system
 

role of nanotechnology in cosmetics

  • 1. IJOPILS. MAR 2015; 3(4):9-19 Vol: 3(4) March 2015 9 www.ijopils.com International Journal of Pharmacy and Integrated Life Sciences “Where improvisation meets innovation” www.ijopils.com REVIEW ARTICLE ISSN: 2320 - 0782 V3-(I4) PG(9-19) Role of Nanotechnology in Cosmetics Aakriti Kapoor1 , Pratibha Nand*1 1. Maharaja Surajmal Institute of Pharmacy, New Delhi, India. ABSTRACT The cosmetic industry is steadily probing for discovery of new formulations with effective delivery system having biological activity. Nanoscience is one of the widely used technologies and finds its applications in the cosmetic industry. Nanotechnology thus is a transformative and new technical revolution and is being used for alteration of physical properties of an enormous range of products from moisturisers, sun blocks, anti-ageing lotions to liquid make up, hair styling and colouring agents, soothing creams etc. However the use of various techniques such as the liposome, niosome, nanocrystals, microemulsion, nanoemulsion, nanosome, nanotubes have their own share of advantages and disadvantages. This article aims at describing some of the nanotechnologies used in the cosmetic industry. KEYWORDS : Cosmetics, liposome, niosomes, nanoemulsions, anti-ageing and sun blocks. Article received on: 11/03/2015 Article accepted on: 28/03/2015 Corresponding Author: Dr. Pratibha Nand Address : Maharaja Surajmal Institute of Pharmacy, New Delhi, India Email : pratibha.msip@gmail.com
  • 2. Nand et. Al. , Volume 3 – Issue 4 Vol: 3(4) March 2015 10 www.ijopils.com INTRODUCTION Nanotechnology is most often described as the manufacture and manipulation of purpose-made structures which are at least smaller than 100nm. The US FDA defines cosmetics, as “articles intended to be rubbed, poured, sprinkled, or sprayed on, introduced into, or otherwise applied to the human body for cleansing, beautifying, promoting attractiveness, or altering the appearance; and articles intended for use as a component of any such articles except that such term shall not include soap1 [FD&C Act, sec. 201]. Cosmetics account to be a paramount constituent of one’s routine life, ranging from the use of moisturisers to toothpastes to perfumes to beauty products. The European commission approximated in the year 2006 that nanoparticles are a constituent of 5% cosmetic products.2 The cosmetics industry therefore uses nano sized formulations thus causing deeper penetration of the agents in the skin, resulting in the protection of sensitive agents, controlled release, reduction in the amount of active molecule and additives, longer shelf life and hence greater product effectiveness. 1, 3 Nanotechnology, a small wonder being explored by scientist in the form of nanomaterials such as niosomes, nanocrystals, nanoemulsions, solid lipid nanoparticles (SLN), and nano structured lipid carriers (NLC), found to give better results than the traditionally used formulations. Nanoparticulate drug delivery system, is gaining lot of attention across biomedical, chemical foods and cosmetics industry, because of its ability to cross the biological barriers, and get accumulated at target site and/or improve the solubility of drugs. It has been reported solid lipid nanoparticles, fullerenes and nanostructure lipid carriers have proved to be better safety vehicles than liposomes because they are capable of providing enhanced skin hydration, better bioavailability and controlled occlusion with improved stability. Consumers using sunscreens without zinc and titanium oxide are exposed to more UVA radiation, with increased risks of skin damage, premature aging, wrinkling, and UV-induced immune system damage. Literature revealed the use of nanoparticles of zinc oxide and titanium dioxide in sunscreens lotions as principal ingredients and was found to be beneficial for giving protection against sun with decreased visibility of the white tinge which is generally observed in conventional compositions.
  • 3. Nand et. Al. , Volume 3 – Issue 4 Vol: 3(4) March 2015 11 www.ijopils.com The present review explores the current state of knowledge on nanotechnology in cosmetics, various potential risks involved to human beings and the measures taken to ensure the development of safe and effective nano-based products in cosmetics. 1. Liposomes Liposomes are spherical, self-closed vesicles containing phospholipid bilayer encapsulating the core material.4 When one bilayer encapsulates the aqueous core it is called unilamellar vesicles while in the case of many concentric bilayers are involved then multilamellar vesicles are formed. 5, 6 Liposomes are generally synthesized with self-hydrolysable lipids which allow time-controlled release of drugs. In addition to the natural lipids, liposomes can also be made from synthetic lipids which include non-ionic surfactant lipids and make them chemically more stable. Liposomes can vary in size, from 15 nm up to several μm and liposomes vesicles in the range of nanometres are called nanoliposomes.2 Recently, a new type of liposomes called transferosomes find their application in cosmetics as they are more elastic than liposomes. 7 Transferosomes size varies in the range of 200-300 nm and can penetrate the skin with improved efficiency than liposomes. Liposomes are actually nano scale lipid based vehicles. Micelles and polymerosomes are other lipid based vehicles. Liposome as drug delivery systems can offer several advantages over conventional dosage forms. These lipid based vehicles are used for increasing the solubility of hydrophobic substances and for limiting the drug toxicity. Liposome provides sustained release and improved penetration into tissues, especially in the case of dermal application. However, several problems have been observed with these traditional vehicles, such as nonspecific uptake, rapid clearance, and instability, which limit the therapeutic potential of these vehicles. Recently certain novel preparations of these compounds have been developed to overcome these problems. Liposomes coated with PEG, known as stealth liposome, are known to increase bioavailability significantly because of reduced, nonspecific uptake. Liposome constructed with novel lipid polymers have resulted in increased membrane stability.8 2. Niosomes
  • 4. Nand et. Al. , Volume 3 – Issue 4 Vol: 3(4) March 2015 12 www.ijopils.com Niosomes are non-ionic surfactant based vesicles having a structure similar to liposomes, formed by the self-assembly of non-ionic surfactants in aqueous media. Initially developed and patented by L’Oréal in mid past 1970’s.9 Niosome entered the market of the cosmetics offering various advantages. “Niosome” introduced in 1987 by Lancôme.Van Hal et al. 10 and they reported that niosome encapsulated estradiol can be delivered through the stratum corneum which is supposed to be a protective barrier. 11, 17 Due to the high chemical stability of the surfactant as compared to the phospholipid and no requirement of special preparation and storage conditions is an advantage of niosomes over the liposomes, which resulted in low manufacturing costs and reduced purity problems. 12 Use of novel surfactant (bola surfactant) for making niosomes has been found effective for percutaneous drug delivery application. During preparation, application of heat or agitation ensures niosomes to attain a closed bilayer structure. 13 The inner aqueous core of the niosome could be used for delivery of the various hydrophobic and hydrophilic drugs such as NSAIDS, anti-inflammatory, anti-infective agents and other classes of drug which offers the biggest advantage of enhancing the transdermal drug delivery. 14, 15, 16 3. Nanoemulsions Due to their unique properties such as their small droplet size, thermodynamic stability, efficient drug delivery system, desirable sensorial and aesthetic properties, the use of less surfactant, nanoemulsions systems continued to attract a great part of cosmetic and pharmaceutical industry.18, 19 .These systems have remarkably uniform and small droplet size which results in optically transparent or a translucent system, moreover their low viscosity leads to good spreadability. Problems associated with the conventional emulsion systems are like creaming, flocculation, sedimentation and coalescence which are not observed with nanoemulsions, making them more acceptable in the cosmetic industry. These systems constitute an effective transport system due to their increased free energy and high surface area. 20 Nanoemulsions may be water in oil, oil in water or a bi-continuous one along with a suitable combination of surfactants or co-surfactants, which is approved for human consumption (GRAS).21 Nanoemulsions are a better choice for transport of lipophilic substances as compared to liposome due to their lipophilic interior and moreover their effective delivery of drug make them popular in the industry. 20
  • 5. Nand et. Al. , Volume 3 – Issue 4 Vol: 3(4) March 2015 13 www.ijopils.com 4. Microemulsions In order to overcome the shortcomings of the prevalent formulations such as thermodynamic instability and limited shelf life, the microemulsions was introduced by Hoar and Schulman in 1943 as potential delivery system. These transparent, isotropic, monophasic systems have distinctive properties like large interfacial area, ultralow interfacial tension, thermodynamic stability, dynamic microstructure , long shelf life, low viscosity , ability to solubilise immiscible liquids and with reasonably lower cost of production when compared to the conventional formulations.18-22, 24 As these systems can consume high amount of lipophilic constituents in the inner oil phase, which is essential component of formulation as it increases their usefulness. Presence of nonpolar, polar and interfacial realm allows enveloping constituents of varying range of solubility.22, 23 Their small droplet size, density and increased surface area makes the droplets clinch with the skin resulting in increased permeation. 24 Microemulsions as skin care product contain tetraethylene glycol monododecyl ether, sodium alkyl sulphate, lecithin, alkyl dimethyl amine oxide, propranolol, hexadecane, isopropyl myristate as their constituents25 . Hair care products also contain amino functional poly organosiloxane and acid or metal salt. 5. Nanocrystals Nanocrystals are clusters of hundreds to tens of thousands of atoms and their size ranges between 10 to 400 nm. The properties of nanocrystals like band gap, charge conductivity, and melting point are dependent on their size and surface area. Nanocrystals have generally been used in the pharmaceutical industry to overcome problems such as poor solubility, low bioavailability and problems with delivery of drugs.26 Nanocrystals are beneficial for the pharmaceutical industry due to their enhanced dissolution velocity, saturation solubility and reproducibility of oral absorption, improved dose bioavailability and increased patient compliance by reducing number of doses.27 The first cosmetic product that appeared in market Juvena in 2007 and La Prairie in 2008 which consisted of two poorly soluble plant antioxidants rutin and hespiridine that previously could not be used for dermal purpose, once formulated as nanocrystals they had became available dermally as per the measured antioxidant effect .2 The first nanocrystals product Rapamune® (rapamycin,
  • 6. Nand et. Al. , Volume 3 – Issue 4 Vol: 3(4) March 2015 14 www.ijopils.com immunosuppressive) was placed on market in year 2000 by Wyeth.26 In 2001, the second product Emend® was introduced by the company Merck (aprepitant capsule, antiemetic), which had a much higher nano crystal loading when compared to Rapamune.28 Nanocrystals generally reduce the dose to be administered and provide a sustained release effect with better patient compliance.2 For their commercial production, pearl milling and high pressure homogenisation can be used which is also accepted by regulatory authorities. The first four marketed products containing nanocrystals such as Rapamune®, Emend®, Tricor® and Megace ES® were prepared by Pearl mill technology by Elannanosystems. 28, 29 6. Dendrimers The term dendrimer has been derived from two Greek words “Dendron” meaning tree and “Meros” meaning part.30- 32 The chemistry of dendrimers was introduced by Fritz Vogtle and co-workers in 1978.30 The dendrimers are three-dimensional, hyper-branched, globular, monodisperse synthetic polymers having well defined shape, molecular weight and size.33 A dendrimer essentially comprises of a central core with branches that are radically attached to the central core 33 and terminal functional group attached to outer series of branches.34 A wide variety of dendrimers are available depending upon the compatibility and other properties. Dendrimers can be prepared by Divergent, Convergent, and Double exponential or mixed methods. 35 Dendrimers have an important contribution in the cosmetic industry, brands such as L’Oreal and Unilever have patents in using dendrimer for the production of mascara, nail polish and sprays, gels and lotions respectively.36-37 Besides these dendrimers have wide variety of applications ranging from therapeutic, diagnostic to pharmaceutical industry. SAFETY CONCERNS One of the most popular questions raised in the media and peer-reviewed articles is “how safe is nanotechnology38 . It has been established that nano sized particles are present in sunscreens and cosmetics and they have raised the issue of safety regarding the dermal penetration of these particles, leading to ill health. Penetration and dermal exposure are important issues when handling engineered nanomaterials. Zinc oxide and titanium dioxide are being used as an effective Ultra- violet blocking agent in sunscreen lotions.39 The point is when these engineered nanomaterials
  • 7. Nand et. Al. , Volume 3 – Issue 4 Vol: 3(4) March 2015 15 www.ijopils.com come in contact with human skin and penetrate through the layers of skin what impact they have on skin. Tinkle et al reported that latex particles of size smaller than one micrometer penetrate outer layers of skin during flexing. Some studies show that presence of healthy intact skin acts as a good barrier against nano structured particles 40 . Ryman Rasmussen et al have reported that quantum dots of different size, shape with coating can penetrate through outer layers of pig skin and enter the epidermis and dermis in 24 hours, the smallest particles (4.6 nm in diameter) had shown localisation in the epidermis and the dermis within period of 8 hours irrespective of the coating material and larger non spherical particles showed a penetration rate dependent on the coating.40 CONCLUSION As nanotechnology moves toward widespread commercialization and it is a transformative technology which is merging with information technology, biology and social science. It is expected to reinvigorate discoveries and innovations in many areas of the economy. Nanomedicine is dominated by nanoparticulate drug delivery systems because of their ability to cross biological barriers.
  • 8. Nand et. Al. , Volume 3 – Issue 4 Vol: 3(4) March 2015 16 www.ijopils.com REFERENCES 1. Adnan A, Mohammad R, Farhan JA, Zeenat IK, Roop KK, Mohammed A and Sushama T. Emerging role of microemulsions in cosmetics ; Recent Patents on Drug Delivery & Formulation. 2008; 2: 275-289. 2. Anju S,Senthil KM, Mahadevan N. Nanotechnology: a promising approach for cosmetics; International Journal of Recent Advances in Pharmaceutical Research. 2012; 2(2): 54-61. 3. Sabine G, André G, Myrtill S, Ulrich F, Michael N. Nanotechnology in cosmetics. Nano trust Dossier No.008n. 2010. 4. Bangham, AD and Horne RW. Negative staining of phospholipids and their structured modofication by surface active agents as observed in the electron microscope. J Mol Biol. 1964; 8: 660–668. 5. Papahadjopoulos D. Liposomes and their use in biology and medicine. NY Acad Sci 1978; 1–412. 6. Lasic DD. Applications of liposomes , Liposome Technology, Inc. 1050 Hamilton Court,Menlo Park, California, USA 94025 7. Cevc G. Transferosomes, liposomes and other lipid suspensions on the skin: permeation enhancement, vesicle penetration, and transdermal drug delivery. Crit Rev Ther Drug Career Syst. 1996; 13: 257–388, 8. Thong HY, Zhai H, Maibach HI. Percutaneous penetration enhancers: An overview. Skin Pharmacol Physiol. 2007; 20, 272–282. 9. Procédé de fabrication de dispersions aqueuses de spérules lipidiques et nouvelles compositions correspondantes, L’Oréal, French Patent 2315991, 1975. 10. Cosmetic and pharmaceutical compositions containing niosomes and a water-soluble polyamide, and a process for preparing these compositions, L’Oréal, US Patent 4830857, 1989. 11. Van H D, Vanrensen A, Devringer T, Junginger H, Bouwstra J, Diffusion of estradiol from non-ionic surfactant vesicles through human stratum-corneum in-vitro. STP Pharm Sci. 1996; 6: 72–78.
  • 9. Nand et. Al. , Volume 3 – Issue 4 Vol: 3(4) March 2015 17 www.ijopils.com 12. Pushpendra KT, Choudary S, Ankur S, Devindera PS, Vikas C. Niosomes: study on noval drug delivery system-A review. International Journal of Pharmaceutical and Research and Development. 2012; 3: 100-106. 13. Paolino D, Muzzalupo R, Ricciardi A, Celia C, Picci N, Fresta M. In vitro and in vivo evaluation of Bola-surfactant containing niosomes for transdermal delivery. Biomed Microdevices. 2007;9: 421–433. 14. Uchegbua IF, Vyas SP. Non-ionic surfactant based vesicles (niosomes) in drug delivery. International Journal of Pharmaceutics. 1998;172: 1-2, 33-70. 15. Reddy DN, Udupa N. Formulation and evaluation of oral and transdermal preparations of flurbiprofen and piroxicam incorporated with different carriers. Drug Dev Ind Pharm. 1993; 19: 843–852. 16. Walker W, Brewer JM, Alexander J. Lipid vesicle-entrapped influenza A antigen modulates the influenza A specific human antibody response in immune reconstituted SCID-human mice. Eur J Immunol. 1996; 26: 1664–1667, 17. Anuradha P, Vandana P. Novel lipid based systems for improved topical delivery of antioxidants. Household and Personal Care today. 2009; 4: 5-8. 18. Amnon C, Sintov and Haim V, Leavy. A microemulsion based delivery system for the delivery of therapeutics. Innovation in Pharmaceutical Technology.2007; 23: 68-72. 19. Danielsson I, Lindman B. The definition of microemulsion. Colloid Surf 1981; 3: 391-392. 20. Narang AS, Delmarre D, Gao D. Stable drug encapsulation in micelles and microemulsions. Int J Pharm. 2007; 345: 9-25. 21. Yuan Y, Li SM, Mo FK, Zhong DF. Investigation of microemulsion system for transdermal delivery of meloxicam. Int J Pharm. 2006; 321: 117-123. 22. Kreilgaard M, Pedersen EJ, Jaroszewski JW. NMR characterization and transdermal drug delivery potential microemulsion systems. J Control Release. 2000; 69: 421-433. 23. Kreilgaard M. Influence of microemulsion on cutaneous drug delivery. Adv Drug Delivery Rev. 2002; 54: S77-S98. 24. Elena P, Paola S, Maria RG. Transdermal permeation of apomorphine through hairless mouse skin from microemulsions. Int J Pharm. 2001; 226: 47-51. 25. Paul BK, Moulik S. Uses and applications of microemulsions. Current Sci. 2001; 80: 25.
  • 10. Nand et. Al. , Volume 3 – Issue 4 Vol: 3(4) March 2015 18 www.ijopils.com 26. Shegokar R, Muller RH.Nanocrystals: Industrially feasible multifunctional formulation technology for poorly soluble actives. Int J Pharm. 2011; 399: 129–139. 27. Müller RH, Krause K, Mäder K. Method for controlled production of ultrafine microparticles and nanoparticles. 2001b:WO/2001/003670 28. Petersen R. Nanocrystals for Use in Topical Cosmetic Formulations and Method of Production Thereof. Abbott GmbH & Co., US Patent 60/866233, 2008. 29. Sanjay B, Meena B, Rachna K. Nanocrystals: Current strategies and trends. Int J Res Pharm Biomed Sci.2012; 3: 406-419. 30. Buhleier E, Wehner W, Vogtle F. Cascade and Nonskid-chain like synthesis of molecular cavity topologies. Synthesis. 1978; 2: 155-158. 31. Tomalia DA, Baker H, Dewald J, Hall M, Kallos G, Martin S, Roeck J, Ryder J, Smith P. A new class of polymers: Starburst- dendritic macromolecules. Polymer Journal, 2006; 17: 117-132. 32. Newkome GR, Yao ZQ, Baker GR, Gupta VK. Cascade molecules: A new approach to micelles, A-arborol. Journal of Organic Chemistry. 1985; 50: 2003-2006. 33. Cheng Y, Tongwen X. Dendrimers as potential drug carriers. Part I. Solubilisation of non- steroidal anti-Inflammatory drugs in the presence of polyamidoamine dendrimers. Eur J Med Chem. 2005; 40: 1188-1192. 34. Caminade AM, Laurent R, Majoral JP. Characterization of dendrimers. Advanced Drug Deliv Rev. 2005; 57: 2130-2146. 35. Sonke S, Tomalia DA. Dendrimers in biomedical application reflection on the field. Advanced Drug Deliv Rev. 2005; 57: 2106-2129. 36. Jean M, Sylvie G. Use of hyper branched polymer and dendrimers comprising a particular group as film- forming agent, film forming composition comprising same and use particularly in cosmetics and pharmaceutics, L’Oreal, U S Patent 6432423, 2002. 37. Delphine A, Serge F. Self- tanning cosmetic composition, L’Oreal, U.S Patent 6399048, 2002. 38. Hood E. Environ. Nanotechnology: looking as we leap. Environmental Health Perspectives Health Perspect. 2004; 112 (13): A741-A749
  • 11. Nand et. Al. , Volume 3 – Issue 4 Vol: 3(4) March 2015 19 www.ijopils.com 39. Popov A P, Priezzhev AV, Lademann J, R Myllyla. TiO2 nanoparticles as an effective UV- B radiation skin-protective compound in sunscreens. J Phys D Appl Phys 2005; 38 (15): 2564-2570. 40. Willander M, Omer N, Lozovik YE, Al-Hilli SE, Chiragwandi Z, QH Hu, Zhao QX, Klason P. Solid and soft nanostructured materials: Fundamentals and applications . Microelectron J. 2005; 36 (11): 940-949.