Innovative Mucoadhesive Precursor of Liquid Crystalline System Loading Anti-Gellatinolytic Peptide for Topical Treatment of Oral Cancer

Current researches report an actual benefit of a treatment for oral cancer via inhibition of proteolytic matrix metallopro-teinases (MPP) with a peptide drug, called CTT1. However, peptides present poor oral bioavailability. Topical administration on oral mucosa avoids its passage through the gastrointestinal tract and the first-pass liver metabolism, but the barrier function of the oral mucosa can impair the permeation and retention of CTT1. The objective of this study is to incorporate CTT1 into a mucoadhesive precursor of liquid crystalline system (PLCS) as an interesting strategy for the topical treatment of oral cancer. PLCS consisting of oleic acid, ethoxylated 20 and propoxylated cetyl alcohol 5, polyethyleneimine (P)-associated chitosan (C) dispersion and CTT1 (FPC-CTT1) was developed and characterized by polarized light microscopy (PLM) and small-angle X-ray scattering (SAXS). In vitro permeation and retention across esophageal mucosa, In vitro cytotoxicity towards tongue squamous cell carcinoma cells, and in vivo evaluation of vascular changes using the chick embryo chorioallantoic membrane (CAM) model were performed. PLM and SAXS showed that FPC-CTT1acted as PLCS, because it formed a lamellar liquid crystalline system after the addition of artificial saliva. FPC-CTT1increased approximately 2-fold the flux of permeation and 3-fold the retention of CTT1 on the porcine esophageal mucosa. CTT1 does not affect cell viability. CAM tests showed that FPC preserved the blood vessels and it can be a safe formulation. These findings encourage the use of the FPC-CTT1 for topical treatment of oral cancer.

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Structural characterization and in vivo evaluation of retinyl palmitate in non-ionic lamellar liquid crystalline system

Colloids and Surfaces B Biointerfaces ◽

10.1016/j.colsurfb.2011.02.027 ◽

2011 ◽

Vol 85 (2) ◽

pp. 182-188 ◽

Cited By ~ 43

Author(s):

M. Chorilli ◽

P.S. Prestes ◽

R.B. Rigon ◽

G.R. Leonardi ◽

L.A. Chiavacci ◽

...

Keyword(s):

Structural Characterization ◽

Liquid Crystalline ◽

Retinyl Palmitate ◽

In Vivo Evaluation ◽

Crystalline System ◽

Liquid Crystalline System

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LYOTROPIC LIQUID CRYSTALLINE SYSTEM FOR EFFECTIVE TOPICAL DELIVERY OF TOLNAFTATE

Asian Journal of Pharmaceutical Research and Development ◽

10.22270/ajprd.v6i3.349 ◽

2018 ◽

Vol 6 (3) ◽

pp. 75-80 ◽

Cited By ~ 1

Author(s):

Jyotsna T Mahajan ◽

Nayan Gujarathi ◽

Anil Jadhav ◽

Vasim Pathan ◽

Lakshmikant Borse

Keyword(s):

Liquid Crystalline ◽

In Vitro Drug Release ◽

Efficient Delivery ◽

Antimycotic Activity ◽

Phase Liquid ◽

Profile Characteristics ◽

Crystalline System ◽

Dermal Drug Delivery ◽

Liquid Crystalline System

The present investigation deals with the formulation, optimization and evaluation of liquid crystalline cream of Tolnaftate. Brij-78 used as a surfactant, Cetostearyl alcohol was used as a co-surfactant and Silicon oil as a oil phase. Liquid crystalline cream system, has a potential for efficient delivery of Tolnaftate (1%), as topical dermal drug delivery system. The liquid crystalline system enhance the diffusion of water insoluble drug Tolnaftate through the skin for effective result. Liquid crystals (LC) are substances that flow like liquids but maintain some of the ordered structure characteristics of crystalline solids. Based on the ways that LCs are generated, they can be classified into two types 1) Thermotropic LCS and 2) Lyotropic LCs. Incorporation of the drug in liquid crystal increased its antimycotic activity against different antifungal microorganisms. Used surfactant enhance the penetration of drug and also improve the solubility of drug. The objective of this study was to increase the diffusion coefficient of drug through the formulation, and also to improve the availability of drug at the site of action. The prepared liquid crystalline cream exhibited the expected, viscosity, drug content, pH, spreadability, in vitro drug release and in vitro antimycotic inhibitory activity. Liquid crystalline cream for tolnaftate was found to be stable cream. It was found to have better in vitrorelease profile characteristics, and in vitro antimycotic activity, it can be concluded that the formulation F5 has better potential of antimicrobial activity and to enhance the diffusion of drug through the cream.

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Terpinen-4-ol and nystatin co-loaded precursor of liquid crystalline system for topical treatment of oral candidiasis

Scientific Reports ◽

10.1038/s41598-020-70085-z ◽

2020 ◽

Vol 10 (1) ◽

Author(s):

Renata Serignoli Francisconi ◽

Patricia Milagros Maquera-Huacho ◽

Caroline Coradi Tonon ◽

Giovana Maria Fioramonti Calixto ◽

Janaína de Cássia Orlandi Sardi ◽

...

Keyword(s):

Topical Treatment ◽

Liquid Crystalline ◽

Oral Candidiasis ◽

Crystalline System ◽

Liquid Crystalline System

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Induction and Differentiation of Dental Epithelium in Vivo and in Vitro

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100053425 ◽

1982 ◽

Vol 40 ◽

pp. 142-145

Author(s):

E. J. Kollar

Keyword(s):

Connective Tissue ◽

Oral Mucosa ◽

Basal Lamina ◽

Functional Derivatives ◽

Specific Source ◽

Dental Epithelium ◽

Connective Tissue Stroma

The differentiation and maintenance of many specialized epithelial structures are dependent on the underlying connective tissue stroma and on an intact basal lamina. These requirements are especially stringent in the development and maintenance of the skin and oral mucosa. The keratinization patterns of thin or thick cornified layers as well as the appearance of specialized functional derivatives such as hair and teeth can be correlated with the specific source of stroma which supports these differentiated expressions.

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Use of light microscopy in the qualitative and quantitative study of liquid crystalline order

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100121727 ◽

1992 ◽

Vol 50 (1) ◽

pp. 264-265

Author(s):

Christopher Viney

Keyword(s):

Light Microscopy ◽

Liquid Crystalline ◽

Structural Characteristics ◽

Molecular Order ◽

Liquid Crystalline Phases ◽

Convenient Technique ◽

Liquid Crystalline Materials ◽

Transparent Windows

Light microscopy is a convenient technique for characterizing molecular order in fluid liquid crystalline materials. Microstructures can usually be observed under the actual conditions that promote the formation of liquid crystalline phases, whether or not a solvent is required, and at temperatures that can range from the boiling point of nitrogen to 600°C. It is relatively easy to produce specimens that are sufficiently thin and flat, simply by confining a droplet between glass cover slides. Specimens do not need to be conducting, and they do not have to be maintained in a vacuum. Drybox or other controlled environmental conditions can be maintained in a sealed chamber equipped with transparent windows; some heating/ freezing stages can be used for this purpose. It is relatively easy to construct a modified stage so that the generation and relaxation of global molecular order can be observed while specimens are being sheared, simulating flow conditions that exist during processing. Also, light only rarely affects the chemical composition or molecular weight distribution of the sample. Because little or no processing is required after collecting the sample, one can be confident that biologically derived materials will reveal many of their in vivo structural characteristics, even though microscopy is performed in vitro.

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Investigation of Phase States, Thermo-Morphologic, Magneto-Morphologic and Refractive Properties of Mesophases in Dodecyltrimethyl Ammonium Bromide – Water Lyotropic Liquid Crystalline System

Tenside Surfactants Detergents ◽

10.3139/113.110470 ◽

2016 ◽

Vol 53 (6) ◽

pp. 524-532 ◽

Cited By ~ 1

Author(s):

Arif Nesrullajev ◽

Pınar Özden

Keyword(s):

Liquid Crystalline ◽

Ammonium Bromide ◽

Crystalline System ◽

Liquid Crystalline System

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Overexpression of the Oral Mucosa-Specific microRNA-31 Promotes Skin Wound Closure

International Journal of Molecular Sciences ◽

10.3390/ijms20153679 ◽

2019 ◽

Vol 20 (15) ◽

pp. 3679 ◽

Cited By ~ 3

Author(s):

Lin Chen ◽

Alyne Simões ◽

Zujian Chen ◽

Yan Zhao ◽

Xinming Wu ◽

...

Keyword(s):

Wound Healing ◽

Oral Mucosa ◽

Wound Closure ◽

Expression Patterns ◽

Skin Wound ◽

Skin Wound Healing ◽

Specific Expression ◽

Keratinocyte Proliferation

Wounds within the oral mucosa are known to heal more rapidly than skin wounds. Recent studies suggest that differences in the microRNAome profiles may underlie the exceptional healing that occurs in oral mucosa. Here, we test whether skin wound-healing can be accelerating by increasing the levels of oral mucosa-specific microRNAs. A panel of 57 differentially expressed high expresser microRNAs were identified based on our previously published miR-seq dataset of paired skin and oral mucosal wound-healing [Sci. Rep. (2019) 9:7160]. These microRNAs were further grouped into 5 clusters based on their expression patterns, and their differential expression was confirmed by TaqMan-based quantification of LCM-captured epithelial cells from the wound edges. Of these 5 clusters, Cluster IV (consisting of 8 microRNAs, including miR-31) is most intriguing due to its tissue-specific expression pattern and temporal changes during wound-healing. The in vitro functional assays show that ectopic transfection of miR-31 consistently enhanced keratinocyte proliferation and migration. In vivo, miR-31 mimic treatment led to a statistically significant acceleration of wound closure. Our results demonstrate that wound-healing can be enhanced in skin through the overexpression of microRNAs that are highly expressed in the privileged healing response of the oral mucosa.

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