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Journal articles on the topic 'Flotting Drug Delivery System'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Ashish, Sonawane* Yashpal More Vaibhav Patil. "Formulation And Assessment of Oral Gel for The Treatment of Mouth Ulcer Using Extract from Jamun Seed Powder." International Journal of Pharmaceutical Sciences 3, no. 5 (2025): 3566–74. https://doi.org/10.5281/zenodo.15478930.

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A new era in the successful creation of controlled release formulations with many properties to offer an effective drug delivery mechanism began with the introduction of bilayer tablets. Bilayer tablets are superior to conventional mouthwash, sprays, and gels. Therefore, using a bilayer pill for analgesic and anti-inflammatory purposes is rather different. Two incompatible substances can be separated using bi-layer tablets, two treatments can be released successively, or sustained release tablets with an immediate release dose in the first layer and a maintenance dose in the second layer can b

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2

Ankit Kumar and Sanjeev Kumar. "Intra Vaginal Drug Delivery System (Novel Drug Delivery System)." International Journal for Research in Applied Sciences and Biotechnology 7, no. 6 (2020): 234–41. http://dx.doi.org/10.31033/ijrasb.7.6.33.

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In case of intra-vaginal route of drug administration the dosage form is applied vaginally for the convenient release of the dosage form and for better therapeutic action of the medicament, it is usually used in HIV patients. many conditions that affect the female reproductive tract, such as , sexually transmitted diseases, fungal & bacterial infections, cancer and various pathogens such as virus (human immunodeficiency virus, HIV), bacteria (Gardnerella vaginalis), fungi (Candida spp.) or parasites (Trichomonas vaginalis). Systemically active drugs (contraceptive steroids) as well as loca

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3

Bhowmik, Debjit, K. P. Sampath Kumar, and Lokesh Deb. "Buccal Drug Delivery System-A Novel Drug Delivery System." Research Journal of Science and Technology 8, no. 2 (2016): 90. http://dx.doi.org/10.5958/2349-2988.2016.00012.7.

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4

SAKURAI, Y. "Drug Delivery System." JAPANES JOURNAL OF MEDICAL INSTRUMENTATION 63, no. 11 (1993): 507–10. http://dx.doi.org/10.4286/ikakikaigaku.63.11_507.

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5

TAKADA, Kanji. "Drug Delivery System." Kagaku To Seibutsu 42, no. 10 (2004): 644–50. http://dx.doi.org/10.1271/kagakutoseibutsu1962.42.644.

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6

Somberg, John C. "Drug Delivery System." Journal of Clinical Pharmacology 29, no. 8 (1989): 673. http://dx.doi.org/10.1002/j.1552-4604.1989.tb03400.x.

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7

Meghana, Raykar, and Shinde Ramesh. "SELF MICROEMULSIFYING DRUG DELIVERY SYSTEM: A LIPID BASED DRUG DELIVERY SYSTEM." INTERNATIONAL JOURNAL OF CURRENT RESEARCH AND INNOVATIONS IN PHARMA SCIENCES 1, no. 1 (2022): 16–21. https://doi.org/10.5281/zenodo.8017592.

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8

Jayprakash, Khandelwal Mohit, Agrawal Dilip, and Goyal Rakesh. "COLON TARGETED DRUG DELIVERY SYSTEM ADVANCE IN NOVEL DRUG DELIVERY SYSTEM." International Journal of Current Pharmaceutical Review and Research 14, no. 03 (2022): 118–23. https://doi.org/10.5281/zenodo.12658882.

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The oral route is considered to be the most preferred route for administration of drugs forsystemic effect, but the oral route is not suitable to the administration of drug for lowergastrointestinal (GI) diseases, this happened due to their release at upper GI tract (stomach,small intestine), which further minimizes the accessibility of drugs at the lower GI tract. Toovercome this difficulty, colon-specific drug delivery systems have been broadly analyzedduring the last two decades. Oral delivery of drugs to the colon is valuable in the treatment ofdiseases of colon (ulcerative colitis, Chron'

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9

Fujiwara, Masahiro. "Drug Delivery System : DDS." Nippon Shokuhin Kagaku Kogaku Kaishi 57, no. 9 (2010): 400. http://dx.doi.org/10.3136/nskkk.57.400.

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10

&NA;. "Copolymer drug delivery system." Inpharma Weekly &NA;, no. 1106 (1997): 9. http://dx.doi.org/10.2165/00128413-199711060-00018.

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11

Rathi, JC, S. Tamizharasi, and V. Rathi. "Floating drug delivery system." Systematic Reviews in Pharmacy 2, no. 1 (2011): 19. http://dx.doi.org/10.4103/0975-8453.83435.

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12

Sivalingan, Giridharan, Ganesh GNK, and Mithra Chandrasekaran. "Multiparticulate Drug Delivery System." Research Journal of Pharmacy and Technology 13, no. 7 (2020): 3501. http://dx.doi.org/10.5958/0974-360x.2020.00620.4.

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13

Thakur, Sanjay, Krishnappa Ramya, Deepak Kumar Shah, and Khadga Raj. "Floating Drug Delivery System." Journal of Drug Delivery and Therapeutics 11, no. 3-S (2021): 125–30. http://dx.doi.org/10.22270/jddt.v11i3-s.4828.

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Floating drug delivery system (FDDS) helps to improve the buoyancy property of the drug over the gastric fluids and hence maintain the longer duration of action. It is helpful in minimizing the dosing frequency. The density of dosage form must be less than the density of gastric contents (1.004 gm/ml) in FDDS. It may effervescent or non-effervescent system. The drugs having narrow absorption window in GIT is good candidate for the floating drug delivery system. The main objective of writing this review article is to compile the recent literature with special focus on classification, method of

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14

Belgamwar, VeenaS, MadhuriV Gaikwad, GaneshB Patil, and Sanjay Surana. "Pulsatile drug delivery system." Asian Journal of Pharmaceutics 2, no. 3 (2008): 141. http://dx.doi.org/10.4103/0973-8398.43297.

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15

heir, Mandeep Kaur, and Sachin Sharma. "Transdermal Drug Delivery System." Indo Global Journal of Pharmaceutical Sciences 09, no. 02 (2019): 155. http://dx.doi.org/10.35652/igjps.2019.92s53.

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16

Yamahara, Hiroshi. "Transdermal Drug Delivery System." MEMBRANE 31, no. 1 (2006): 40–41. http://dx.doi.org/10.5360/membrane.31.40.

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17

Goud, M. Sharath Chandra, and V. P. Pandey. "GASTRORETENTIVE DRUG DELIVERY SYSTEM." International Journal of Pharmacy and Biological Sciences 6, no. 3 (2016): 158–65. http://dx.doi.org/10.21276/ijpbs.2016.6.3.19.

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18

McHugh, Jessica. "Promising drug delivery system." Nature Reviews Rheumatology 15, no. 2 (2019): 64. http://dx.doi.org/10.1038/s41584-019-0158-1.

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19

Dhamore, Harshada Gorakh, Assist Prof Kalpana S. Kale, and Dr Megha Salve. "Liposomal Drug Delivery System." International Journal of Pharmaceutical Research and Applications 09, no. 06 (2024): 502–9. https://doi.org/10.35629/4494-0906502509.

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Liposomes have been considered promising and versatile drug vesicles. Compared with traditional drug delivery systems, liposomes exhibit better properties, including site-targeting, sustained or controlled release, protection of drugs from degradation and clearance, superior therapeutic effects, and lower toxic side effects. Given these merits, several liposomal drug products have been successfully approved and used in clinics over the last couple of decades. In this review, the liposomal drug products approved by the U.S. Food and Drug Administration (FDA) and European Medicines. Agency (EMA)

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20

Swetha, Dr M., Makka Vandana, Mandugula Shiva Nandini, and Manumari Vaishnavi. "Implantable Drug Delivery System." International Journal of Multidisciplinary Research and Growth Evaluation 6, no. 1 (2025): 1578–82. https://doi.org/10.54660/.ijmrge.2025.6.1.1578-1582.

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Implantable drug delivery systems [IDDS] provide a viable substitute for conventional medication delivery techniques. The most popular medication delivery methods, oral and injectable, frequently cause blood drug concentrations to peak and then fall. This calls for ongoing administration in order to sustain therapeutic medication levels. Oral medication distribution also has to contend with issues such first-pass metabolism and drug degradation in the gastrointestinal system. Conversely, IDDS allow for prolonged medication release, which makes them particularly useful for treating chronic illn

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21

Kim, Jin-Seok. "Liposomal drug delivery system." Journal of Pharmaceutical Investigation 46, no. 4 (2016): 387–92. http://dx.doi.org/10.1007/s40005-016-0260-1.

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22

Suryawanshi, Dr Amrata D. "Transdermal Drug Delivery System." International Journal for Research in Applied Science and Engineering Technology 11, no. 10 (2023): 858–62. http://dx.doi.org/10.22214/ijraset.2023.56109.

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Abstract: A various non-invasive administration have recently emerged as an alternative toconventional needles. Transdermal drug delivery system is most attractive method. The transdermal as route has numerous advantages over the more traditional drug delivery system and they include high bioavailability, absence offirst pass hepatic metabolism, steady drug plasma concentration. and the fact that therapy is noninvasive. TDDS could be applicable in not only Pharmaceuticals but also in the skin industry, including cosmetics. Transdermal drug delivery has made an important contribution to medical

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23

M Shabbir, M. Sohil, Shaikh Imran Kalam, Dr G. J. Khan, Shaikh Md Moiz, and Shaikh Aman. "Targeted Drug Delivery System." International Journal of Research in Pharmacy and Allied Science 04, no. 01 (2025): 01–19. https://doi.org/10.71431/ijrpas.2025.4101.

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Paul Ehrlich's idea of a "magic bullet" has evolved into Nano medicine. In order to circumvent the particular harmful effect of traditional drug distribution, targeted drug delivery reduces the amount of drug needed for therapeutic efficacy by delivering the drug moiety directly to the specified body location (organ, cellular, and subcellular level of specific tissue). The idea of a "magic bullet" was developed to achieve this aim, and after more than a century of research, scientists created a number of devices that are nanometers in size, which is known as "Nano medicine." Among the carrier

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24

Sayali, shankhapal* Vaishnavi pandav Rutuja jaiswal Sonali kalam. "Transdermal Drug Delivery System." International Journal of Pharmaceutical Sciences 2, no. 8 (2024): 3570–80. https://doi.org/10.5281/zenodo.13354827.

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Transdermal drug delivery systems, or TDDSs, are adhesive patches applied to the skin with a precise dosage that are then absorbed into the bloodstream. It is important to take into account the entire morphological, biophysical, and physicochemical aspects of the skin when delivering medicinal substances through the human skin for systemic effects. A transdermal patch offers a regulated release and continuous drug administration, which is advantageous over other forms of pharmaceutical delivery. It also avoids pulsed entry into the systemic circulation, which frequently results in undesirable

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25

Yogita, Pawar* Shubhangi doer Priti Kolte Nitin kale. "Implantable Drug Delivery System." International Journal of Pharmaceutical Sciences 2, no. 8 (2024): 3684–88. https://doi.org/10.5281/zenodo.13369182.

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Implantable drug delivery system [IDDs] in modern medicine may traced to Deans by and Parkes who in 1938. The oral route is popular and convenient means of drug delivery . with there advantage there is also challenges. many drug are not suitable for the oral route of administration such as insulin. this article gives an overview of classification of these drug delivery devices ;the mechanism of drug release ;the materials used for manufacture. Implants are small sterile solid masses consisting of highly purified drug made by compression or molding or extrusion. Implants are developed with a vi

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26

Shubhangi, Jadhav* Rekha Gunja varsha aher Sonali kalam. "Niosomal Drug Delivery System." International Journal of Pharmaceutical Sciences 2, no. 8 (2024): 3689–96. https://doi.org/10.5281/zenodo.13370938.

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Niosomes (NS) are nonionic surfactant-based vesicles that are biodegradable, nontoxic, and stable drug carrier systems. NS amphiphilic nature makes them effective for encapsulation of lipophilic and hydrophilic active pharmaceutical  ingredient . The method of manufacture, the kind and quantity of surfactant, the concentration of drugs, the concentration of cholesterol, the temperature, and the kind of hydration media can all have an impact on the qualities of NS. When it comes to enhancing patient compliance, lowering side effects, achieving sustained release characteristics, lowering do

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27

Patel, Arshiya Mustak* Quazi Majaz Gulam Javed Khan. "Nasal Drug Delivery System." International Journal in Pharmaceutical Sciences 2, no. 3 (2024): 803–27. https://doi.org/10.5281/zenodo.10853329.

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Nasal route is alternative to parenteral therapy and also useful for long term therapy. Nasal route is non invasive, widely used for the local treatment may also be used for systemic therapy as drug directly goes in systemic circulation. In this article an overview of intranasal drug delivery with its various aspects like factors affecting nasal absorption are discussed. The use of the nasal route for the delivery of challenging drugs such as small polar molecules, vaccines, hormones, peptides and proteins has created much interest in nowadays. Due to the high permeability, high vasculature, l

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28

Vishakha, Shinde* Gayatri Dalvi Trupti Shinde. "Nanomedicine Drug Delivery System." International Journal of Scientific Research and Technology 1, no. 11 (2024): 51–58. https://doi.org/10.5281/zenodo.14160347.

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Nanomedicine and Nano delivery systems are a relatively new but rapidly developing science where materials in the nanoscale range are employed to serve as means of diagnostic tools or to deliver therapeutic agents to specific targeted sites in a controlled manner. Nanotechnology offers multiple benefits in treating chronic human diseases by site-specific, and target-oriented delivery of precise medicines. Drug delivery to certain target cells is now available by using nanoparticles via nanotechnology, Biomedical nanomaterials are used in vivo and in vitro in the clinical researches, because of

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29

Abjel, A.* Gopi S. Sukesh Kumar. "Smart Drug Delivery System." International Journal in Pharmaceutical Sciences 1, no. 10 (2023): 31–43. https://doi.org/10.5281/zenodo.8418711.

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SDDS is a medicine delivery strategy that attempts to increase dosage in specific body areas while increasing therapeutic efficacy and decreasing adverse effects. It addresses issues such as pharmaceutical solubility constraints, degradation, quick clearance rates, non-specific toxicity, and biological barriers. Smart drug delivery methods include nanoparticles, liposomes, vesicles, implants, polymer-based systems, PH-responsive systems, nanoplatforms, and tailored systems. Nanoparticles contain organic and inorganic features, whereas liposomes are used in cancer therapy, anti-inflammatory the

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30

D., Reshma banu* E. Anusha G. Padma K. Akhila S. Fasiya. "Ocular Drug Delivery System." International Journal of Pharmaceutical Sciences 2, no. 12 (2024): 286–302. https://doi.org/10.5281/zenodo.14267024.

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The human eye is a sophisticated organ with distinctive anatomy and physiology that hinders the passage of drugs into targeted ophthalmic sites. Effective topical administration is an interest of scientists for many decades. Their difficult mission is to prolong drug residence time and guarantee an appropriate ocular permeation. Several ocular obstacles oppose effective drug delivery such as precorneal, corneal, and blood-corneal barriers. Routes for ocular delivery include topical, intravitreal, intraocular, juxtascleral, subconjunctival, intracameral, and retrobulbar. More than 95% of market

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Dr., C. S. Parameswari* Gonuguntla Sreevani. "Mucosal Drug Delivery System." International Journal of Pharmaceutical Sciences 2, no. 12 (2024): 632–46. https://doi.org/10.5281/zenodo.14293571.

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Mucoadhesive drug delivery systems interact with the mucus layer covering the mucosal epithelial surface, and mucin molecules and increase the residence time of the dosage form at the site of absorption. The drugs which have local action or those which have maximum absorption in gastrointestinal tract (GIT) require increased duration of stay in GIT. Thus, mucoadhesive dosage forms are advantageous in increasing the drug plasma concentrations and also therapeutic activity. In this regard, this review covers the areas of mechanisms and theories of mucoadhesion, factors influencing the mucoadhesi

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32

Dr., C. S. Parameswari. "Gastroretentive Drug Delivery System." International Journal of Pharmaceutical Sciences 2, no. 12 (2024): 647–58. https://doi.org/10.5281/zenodo.14293650.

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In recent years Gastro retentive drug delivery system has gained researcher’s in the field of oral drug delivery. Various GRDDS approaches can be utilized to retain the dosage forms in the stomach and to releases the drug slowly for an extended period of time. GRDDS can be used to prolong the residence time of delivery system in the stomach. This results in targeting of drug release at a specific site for the systemic or local effects. GRDDS can be used to overcome challenges associated with conventional oral dosage forms and to release the drug at a specific absorption site to improve b

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33

D., Reshma Banu* Kuruva Akhila E. Anusha G. Padma S. Fasiya. "Intrauterine Drug Delivery System." International Journal of Pharmaceutical Sciences 2, no. 12 (2024): 1398–413. https://doi.org/10.5281/zenodo.14387938.

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Writing this overview of intrauterine drug delivery systems was done with the intention of gathering the most recent research, paying particular attention to the many intrauterine techniques that have emerged as the most effective methods for site-specific oral controlled release drug delivery. To end the pregnancy, the medication releases in the uterus. Details about the benefits and drawbacks of IUDDS are provided. IUDs, or intrauterine devices, are used in intrauterine medication delivery systems. They come in a variety of forms and, depending on the type, can be effective for three to 10 y

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34

Pranav, Shinde* Rekha Goukonde Dr. Gajanan Sanap. "Implantable Drug Delivery System." International Journal of Pharmaceutical Sciences 3, no. 1 (2025): 659–70. https://doi.org/10.5281/zenodo.14628080.

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In this paper, we present a shape-programmable magnetically actuated soft capsule robot for semiim plan table drug delivery applications. The shape of the proposed soft capsule is changed by an external magnetic field. To change the robot shape by an external permanent magnet, the relevant soft robot design features and required conditions are investigated using simulations and experiments. If the magnetic field is increased above a critical value, the capsule collapses to a sphere-like stable shape, which keeps the capsule inside the stomach all the time, and it cannot move to the duodenum by

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35

Narinder, Singh* Pooja Devi Muskan Sharma Naval Singh. "Novel Drug Delivery System." International Journal of Pharmaceutical Sciences 3, no. 5 (2025): 434–46. https://doi.org/10.5281/zenodo.15334655.

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The advancement of pharmaceutical sciences has led to the development of various novel drug delivery systems (NDDS) that improve the efficacy, safety, and patient compliance of therapeutic agents. Traditional drug administration methods often encounter challenges such as poor bioavailability, non-specific distribution, and the need for frequent dosing. To overcome these limitations, several innovative approaches have been explored. Transdermal drug delivery systems (TDDS) allow for sustained drug release through the skin, bypassing first-pass metabolism. Vesicular drug delivery systems (VDDS),

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36

Dave, Viny, and Ashwani Mishra. "A Review on Promising Novel Drug delivery System - Bioadhesive Drug Delivery System." Current Research in Pharmaceutical Sciences 7, no. 3 (2017): 69–78. http://dx.doi.org/10.24092/crps.2017.070301.

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37

., Bhupinder Kaur, and Monika Sharma . "Self-Microemulsifying Drug Delivery System- A Recent Approach in Drug Delivery System." Journal of Current Pharma Research 8, no. 4 (2018): 2504–13. http://dx.doi.org/10.33786/jcpr.2018.v08i04.003.

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38

Rajiv Kumar, Rohit Kumar Chopra, Harpreet Singh, Parminder Nain, and RK Dhawan. "Gastro-retentive drug delivery system: A better approach of drug delivery system." Magna Scientia Advanced Biology and Pharmacy 4, no. 1 (2021): 025–34. http://dx.doi.org/10.30574/msabp.2021.4.1.0045.

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The oral route is the best and most popular route for the administration of drugs in the systemic circulation. There are number of drugs which are given through the oral route. Gastro-retentive drug delivery system is very important system for the drug delivery system. The gastro-retentive drugs prolonged the drug time in the git and also improve their their bioavailability. These are widely used for site specific for the treatment of git disorders and diseases. There are number of approaches for gastro retentive drug delivery system such as floating system, mucoadhesive system, swelling syste

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39

Singh, Anupama, Rishabha Malviya, and Pramod K. Sharma. "Pulmonary Drug Delivery System: A Novel Approach for Drug Delivery." Current Drug Therapy 6, no. 2 (2011): 137–51. http://dx.doi.org/10.2174/157488511795304930.

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40

SWETHA, T* MRS.TANUSH REE CHAKRABORTY. "NANOSPONGES: NEW COLLOIDAL DRUG DELIVERY SYSTEM FOR TOPICAL DRUG DELIVERY." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES o6, no. 02 (2019): 4263–76. https://doi.org/10.5281/zenodo.2574445.

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<em>The advent of nanotechnology lead to invention of many dosage forms. Effective targeted drug delivery systems have been a dream for a long time, due to several major drawbacks, a practical approach has been developed for the formation of discrete functionalized particles, which have been termed as ‘Nanosponge’. The development of new colloidal carrier called Nanosponges has the potential to solve these problems. Nanosponge is a novel and emerging technology it can precisely control the release rates of controlled drug delivery for topical use. The invention of Nanosponges has b

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41

Eisha, Ganju Rajni Dubey Anna Ruth Thomas Bhaskar Kumar Gupta. "Invasomes A Novel Drug Delivery for Transdermal Drug Delivery System." International Journal of Pharmaceutical Sciences 3, no. 4 (2025): 1607–14. https://doi.org/10.5281/zenodo.15205214.

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Invasomes are a novel class of elastic phospholipid vesicles designed to enhance the percutaneous penetration of drugs, offering an improved alternative to conventional liposomes. These vesicles are composed of phosphatidylcholine, ethanol, and a variety of terpenes, which are known to significantly enhance skin penetration. Terpenes, such as citral, limonene, and cineole, disrupt the stratum corneum lipids, interact with intracellular proteins, and improve the partitioning of drugs into the skin, facilitating better drug absorption. Ethanol further enhances the vesicle's ability to penetrate

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42

Priya, Agrawal Dilip, and Khandelwal Mohit. "A NOVEL APPROACH IN GASTRO RETENTIVE DRUG DELIVERY SYSTEM: FLOATING DRUG DELIVERY SYSTEM." International Journal of Current Pharmaceutical Review and Research 14, no. 03 (2022): 91–98. https://doi.org/10.5281/zenodo.12658753.

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The purpose of writing this review on gastro retentive drug delivery systems was to compilethe recent literature with special focus on various gastro retentive approaches that haverecently become leading methodologies in the field of site-specific orally administeredcontrolled release drug delivery. In this review, the current technological developments ofFDDS and marketed products have been discussed. In addition, the pharmaceutical basis oftheir design, their advantages and future potential for oral controlled drug delivery arediscussed. 

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43

Ghule, Arpan R., Dattatraya M. Shinkar, and Ravindra B. Saudagar. "Oral Strip Drug Delivery System." Research Journal of Pharmacy and Technology 8, no. 1 (2015): 85. http://dx.doi.org/10.5958/0974-360x.2015.00017.7.

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44

Mishra, Amul, Ridhi Panola, and A. C. Rana. "Microemulsions: As drug delivery system." Journal of Scientific and Innovative Research 3, no. 4 (2014): 467–74. http://dx.doi.org/10.31254/jsir.2014.3412.

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Microemulsions are excellent candidates as potential drug delivery systems because of their improved drug solubilization, long shelf life, and ease of preparation and administration. The formulation of microemulsion for pharmaceutical use requires a thorough understanding of the properties, uses, and limitations of microemulsion. Three distinct microemulsions – oil external, water external and middle phase can be used for drug delivery, depending upon the type of drug delivery upon the type of drug and the site of action. In this article, Since the term ‘microemulsion’ was first coined almost

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45

Dawange, Shreya R., Sahebrao S. Boraste, Prashant L. Pingale, and Sunil V. Amrutkar. "Nanofibers in Drug Delivery System." Asian Journal of Pharmaceutical Research and Development 9, no. 4 (2021): 151–57. http://dx.doi.org/10.22270/ajprd.v9i4.1011.

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The possible applications of electrospun fibers in drug delivery systems (DDS) are critically examined in this study. Nanofibers are among the most desirable resources in some kind of a variety of scenarios due to their operational capabilities including valuable features for another young generation of resources in energy, climate, even wellness. Because of its possibility to synthesize polymers with specific functions like greater porous design electrospinning was already presented as the most effective technique for fabricating polymer-based nanostructures. Electrospinning has emerged with

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46

., V. B. Kadam, K. B. Dhanawade ., V. A. Salunkhe ., and A. T. Ubale A. T. . "Nanoparticle - Novel Drug Delivery System." Journal of Current Pharma Research 4, no. 4 (2014): 1318–35. http://dx.doi.org/10.33786/jcpr.2014.v04i04.009.

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47

Singh, Shikha Y., Smita S. Aher, and Ravindra B. Saudagar. "Ethosomes –Novel Drug Delivery System." Research Journal of Topical and Cosmetic Sciences 6, no. 1 (2015): 7. http://dx.doi.org/10.5958/2321-5844.2015.00002.3.

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48

HIRANO, Jiro, and Hidehiko HIBINO. "Drug Delivery System of Lipids." Journal of Japan Oil Chemists' Society 37, no. 10 (1988): 864–71. http://dx.doi.org/10.5650/jos1956.37.864.

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YOKOYAMA, Kazumasa, and Yasuo UEDA. "Drug Delivery System Using Lipids." Journal of Japan Oil Chemists' Society 43, no. 11 (1994): 994–1000. http://dx.doi.org/10.5650/jos1956.43.994.

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50

Mullaicharam, AR. "Nanoparticles in drug delivery system." International journal of Nutrition, Pharmacology, Neurological Diseases 1, no. 2 (2011): 103. http://dx.doi.org/10.4103/2231-0738.84194.

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