scholarly journals ANTI-ACNE GEL OF ISOTRETINOIN: FORMULATION AND EVALUATION

2017 ◽  
Vol 10 (11) ◽  
pp. 257 ◽  
Author(s):  
Shreya Nikam
Keyword(s):  
Acne Vulgaris ◽  
Skin Irritation ◽  
Butylated Hydroxytoluene ◽  
Diffusion Method ◽  
Diffusion Study ◽  
Formulation Development ◽  
Batch Release ◽  
In Vitro Diffusion ◽  
Gel Formulations

Objective: Isotretinoin is a very effective drug in the treatment of acne vulgaris by topically. The objective of present study was formulation development of anti-acne gel using Isotretinoine and span 80 for topical delivery to cure nodulosystic acne vulgaris. Furthermore, the comparative study of all the evaluation parameters done with marketed formulation of same drug.Methods: Formulation of anti-acne gel of isotretinoin using Carbopol 940 as a polymer and incorporating isotretinoin in form of topical semi-solid gel using magnetic stirrer, Cremophor RH 40, and butylated hydroxytoluene. Drug was uniformly dispersed in Cremophor RH 40 and the respected solvents. Ethanol, isopropyl alcohol, and glycerin were used as solvents in 15% quantity. Further, the formulation was evaluated for physicochemical evaluation of gel formulations. The prepared gel were optimized statistically and characterized for pH, spredability, drug content, viscosity, in vitro diffusion study, acute skin irritation test, and antimicrobial activity. Evaluation test was also compared with marketed formulation of isotretinoin, that is, Sortet gel. The antibacterial and anti-acne activity of different formulations was determined by modified agar well diffusion method on the culture of Propionibacterium acne also compared with marketed formulation.Results: The optimized batch (B10) showed highest spreadability (32.422 g/cm3) in all formulations and also have high percentage of drug contents (95.60%). The spreadability value was 17.998 g/cm3 showing good spreadability. The viscosity of optimized batch was observed less as compared to other formulations, ultimately showed releases also more. In the in vitro diffusion study, B10 batch release 85.69% of the drug as compared to Sotret gel. The antibacterial activity was studied on anaerobic microorganism P. acne, compared with marketed Sortet gel. Optimized batch showed maximum zone of inhibition to P. acne below marketed formulations and standard benzyl peroxide gel.Conclusion: The topical anti-acne gel of isotertinoin was successfully formulated and evaluated for different parameters. The results indicate that the active component, that is, isotertinoin is more effective when subjected in gel formulations and produces effective anti-acne activity in the management of nodulosystic acne vulgaris.

A novel plaster containing benzoyl peroxide microsponges: Formulation, development and evaluation

2020 ◽  
pp. 152808372098046
Author(s):  
Nihal Atabay ◽  
Ayse Merih Sariişik ◽  
Sinem Yaprak Karavana ◽  
Seda Rençber
Keyword(s):  
Benzoyl Peroxide ◽  
Acne Vulgaris ◽  
Skin Irritation ◽  
Active Agent ◽  
Woven Fabric ◽  
Diffusion Method ◽  
Size Analysis ◽  
Vapor Permeability ◽  
Formulation Development

Benzoyl peroxide is a widely used active agent for acne vulgaris treatment that has antibacterial, anti-inflammatory, keratolytic and wound-healing properties. The common complaints for benzoyl peroxide are skin irritation and dryness. To reduce these side effects, microsponge formulations are used as an effective tool in pharmaceutical and cosmetic industries. In this study, a medical plaster was developed containing benzoyl peroxide microsponges which gives an opportunity to explore the potential of the microsponge systems in textile industry. Benzoyl peroxide microsponge was obtained by using quasi-emulsion solvent diffusion method and characterized by SEM, FT-IR, particle size analysis and porosity studies. The microsponges were applied onto 100% cotton woven fabric by using dip-coating technique. In the treatment solution, different binding agents as acrylic binder, and cross-linking agents as poly(ethylene glycol) diglycidyl ether and 1,2,3,4-butanetetracarboxylic acid were used. Microsponges were around 78.4 µm in diameter and had a spherical porous surface. SEM analyses of the treated fabrics proved that the microsponges were succesfully transferred on cotton fabrics. The drug contents of the fabrics containing Benzoyl peroxide loaded microsponge were found to be within the range of 68.512–102.873%. The in vitro drug release results show that the release from both samples was more than 40% within 6 h. The water vapor permeability of plaster prepared with acrylic binder (S1) was significantly higher than the other plasters. This study presents a novel approach for acne treatment based on textiles containing microsponges. The results revealed that microsponges had a promising potential in textile field.

scholarly journals TERMINALIA ARJUNA TRANSDERMAL MATRIX FORMULATION CONTAINING DIFFERENT POLYMER COMPONENTS

2019 ◽  
pp. 266-270 ◽  
Author(s):  
DINANATH GAIKWAD ◽  
NAMDEO JADHAV
Keyword(s):  
Ex Vivo ◽  
Skin Irritation ◽  
Research Work ◽  
Bark Extract ◽  
Terminalia Arjuna ◽  
Diffusion Study ◽  
Matrix Formulation ◽  
Transdermal Patches ◽  
In Vitro Diffusion

Objective: The objective of this research work was to prepare a transdermal matrix formulation containing different polymer components for topical delivery. Methods: Terminalia arjuna bark extract loaded transdermal patches were prepared using solvent casting technique with different amount of chitosan and Eudragit RL 100 batches were prepared according to 32 factorial designs. Results: The transdermal patches prepared were evaluated for different physicochemical properties, determination of drug content, in vitro diffusion study, ex vivo study, skin irritation study, and stability study. Infrared studies indicate the absence of chemical interaction or any changes in the chemical composition of extract during the preparation of transdermal patch. In vitro diffusion study and ex vivo diffusion study of optimized batch S3 showed drug releases to 74.56–69.12%, respectively, up to 12 h. Skin irritation study indicates that the extract and excipients used in the patch do not show any irritating effect on the skin. All the prepared transdermal matrix formulations were found to be stable on storage. Conclusion: It can be concluded that prepared matrix formulation containing different polymer components can be used for transdermal delivery for the treatment of chronic ailments such as cardiovascular disorder.

Development and Evaluation of Particulate Microcarriers of Adapalene as a Topical Delivery System

2019 ◽  
Vol 9 (3) ◽  
pp. 222-233
Author(s):  
Divya D. Jain ◽  
Namita D. Desai
Keyword(s):  
Patient Compliance ◽  
Targeted Delivery ◽  
Ex Vivo ◽  
Acne Vulgaris ◽  
Drug Loading ◽  
Topical Therapy ◽  
Skin Irritation ◽  
Topical Delivery ◽  
Diffusion Method ◽  
Topical Gel

Background: Adapalene is a promising third generation retinoid used in the topical treatment of acne vulgaris. However, the major drawback associated with conventional topical therapy of Adapalene is the ‘retinoid reaction’ which is dose-dependent and characterized by erythema, scaling and burning sensation at the application sites. Microparticulate drug delivery can play a major role in reducing side effects and providing better patient compliance due to targeted delivery. Methods: Adapalene microparticles were prepared using quasi emulsion solvent diffusion method. The effects of formulation variables including polymer ratios, amounts of emulsifier, drug loading and process variables such as stirring time and speed on the physical characteristics of microparticles were investigated. The developed microparticles were characterized by DSC and SEM. Adapalene microparticles were incorporated into Carbopol 971 NF gel for ease of topical delivery. Results: Adapalene microparticulate topical gel showed sustained drug release over 8 hours in in vitro studies. The amount of drug retained in the rat skin during ex vivo studies was higher in the microparticulate topical gel (227.43 ± 0.83 µg/cm2) as compared to the marketed formulation (81.4 ± 1.11 µg/cm2) after 8 hours indicating localized and sustained drug action that can be useful in treating acne vulgaris. The safety of optimized Adapalene gel determined by skin irritation studies performed on Sprague Dawley rats showed no irritation potential. Conclusion: Microparticles can provide promising carrier systems to deliver Adapalene, improving patient compliance due to enhanced skin deposition, localized and sustained action with reduced associated irritant effects.

scholarly journals Evaluation of antipsoriatic activity of gel containing Pongamia pinnata extract on Imiquimod-induced psoriasis

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Kamlesh Wadher ◽  
Shital Dabre ◽  
Anjali Gaidhane ◽  
Sagar Trivedi ◽  
Milind Umekar
Keyword(s):  
Mouse Model ◽  
Pongamia Pinnata ◽  
Gelling Agent ◽  
Proper Treatment ◽  
Phytochemical Screening ◽  
Diffusion Studies ◽  
In Vitro Diffusion ◽  
Gel Formulations ◽  
Disease And Disorders

Abstract Background Pongamia pinnata (Fabaceae) is among those categories of plants mentioned in Ayurveda and traditionally known to use in several types of disease and disorders. The objective of the present work was to investigate the anti-psoriatic activity of Pongamia pinnata leaves extracts in Herbal gel formulation. Results Hydroalcoholic leaves extract of Pongamia pinnata was first subjected to phytochemical screening and quantification of phytoconstituents. Herbal gel was prepared containing Pongamia pinnata extracts using Carbopol 934 as gelling agent. The prepared gel formulations were studied for pH, viscosity, Spreadability and in vitro diffusion studies. The imiquimod-induced psoriatic mouse model, showed a prominent anti-psoriatic activity of the extract as evident through index grading. Treatment with extract confirmed a noteworthy reduction in psoriasis in the treated groups as there was a considerable diminution in the thickness and scaling of skin. Conclusions Lack of proper treatment and disadvantages associated with allopathic medicines pave the way to extensive research in natural products with anti-psoriatic activity. The present research scientifically justified the anti-psoriatic activity of the Hydroalcoholic extracts of Pongamia pinnata leaves.

scholarly journals FORMULATION DEVELOPMENT AND EVALUATION OF PRONIOSOMAL GEL OF ETHINYLESTRADIOL AND LEVONORGESTREL FOR ANTIFERTILITY TREATMENT

2019 ◽  
Vol 12 (1) ◽  
pp. 364
Author(s):  
Shikha Baghel Chauhan ◽  
Tanveer Naved ◽  
Nayyar Parvez
Keyword(s):  
Optical Microscopy ◽  
Encapsulation Efficiency ◽  
In Vitro Release ◽  
Stability Studies ◽  
Formulation Development ◽  
Promising Alternative ◽  
Size And Shape ◽  
Permeation Studies ◽  
Gel Formulations

Objective: The purpose of this research was to develop and formulate proniosomal gel drug delivery system of ethinylestradiol and levonorgestrel for antifertility treatment that is capable of efficiently delivering entrapped drug over an extended period of time.Methods: Ethinylestradiol and levonorgestrel are encapsulated in various formulations of proniosomal gel composed of various ratios of span surfactant, cholesterol, soya lecithin, and alcohol as aqueous phase prepared by coacervation-phase separation method. The prepared formulations characterized for drug encapsulation efficiency, size distribution, in vitro release studies, and vesicular stability at different storage conditions were carried. Stability studies for proniosomal gel were carried out for a few weeks. Morphological size and shape of the vesicles are characterized using optical microscopy and scanning electron microscopy (SEM). Stability studies for proniosomal gel were carried out for 3 months.Results: Morphological size and shape of the vesicles are characterized using optical microscopy and SEM, particles are found to be spherical, size of the particles is in the range of 46.4–80.6 nm, and permeation studies showed good control release for prolonged period of time. The encapsulation efficiency of proniosomal gel formulations is in the range of 74–80% and in vitro permeation studies proved that good amount of drug is permeated and has reasonably good stability characteristics as well.Conclusions: The results suggest that proniosomal gel formulations of ethinylestradiol and levonorgestrel may be used for transdermal delivery for antifertility treatment. The dried proniosomal formulation could act as a promising alternative to niosomes.

scholarly journals FORMULATION AND EVALUATION OF TOPICAL HERBAL GEL CONTAINING INCLUSION COMPLEX OF CURCUMIN

2019 ◽  
pp. 196-201
Author(s):  
VANDANA D ◽  
SHWETA PAWAR
Keyword(s):  
Inclusion Complex ◽  
Protein Denaturation ◽  
Release Kinetics ◽  
Inflammatory Activity ◽  
In Vitro Dissolution ◽  
Diffusion Method ◽  
Topical Gel ◽  
In Vitro Diffusion ◽  
Anti Inflammatory

Objective: The current work was aimed to prepare a topical gel containing curcumin (CUR) for the treatment of microbial infections on skin. Methods: CUR was complexed with the β-cyclodextrin (β-CD) using kneading method in 1:1, 1:2, and 1:3 molar ratios and characterized. The inclusion complex with high aqueous solubility was loaded in the topical gel containing (2% CUR) which was prepared using carbopol, sodium CMC, and guar gum and evaluated for viscosity, spreadability, extrudability, pH, drug content, and in vitro diffusion studies. The in vitro anti-inflammatory activity of the gel was performed by albumin protein denaturation technique, the statistical analysis was done using ANOVA followed Dunnett’s t-test. The antimicrobial activity of CUR was evaluated using standard strains of Candida albicans and Escherichia coli by agar well diffusion method. Results: The complexation of CUR had an increased solubility up to 103.09 times for 1:3 molar ratio with in vitro dissolution 90.64% for 60 min. The optimized formulation F9 had viscosity of 6500.3 cps and 97.5% in vitro drug diffusion for 8 h which follows zero-order release kinetics. In vitro anti-inflammatory activity studied showed that the CUR gel has a good potency for renaturation and was as effective as standard diclofenac with 76.9% inhibition (p=0.0507). CUR showed approx. 3 mm diameter of zone of inhibition against C. albicans and E. coli. Conclusion: A stable topical gel of CUR using β-CD and carbopol was successfully prepared which showed better in vitro diffusion with promising anti-inflammatory and antifungal action.

scholarly journals FORMULATION AND EVALUATION OF GLIBENCLAMIDE GEL FOR TRANSDERMAL DRUG DELIVERY

2020 ◽  
pp. 35-39
Author(s):  
NOSHEEN ANWAR ◽  
SYED UMER JAN ◽  
REHMAM GUL
Keyword(s):  
Oleic Acid ◽  
Skin Irritation ◽  
In Vitro Release ◽  
Acid Effect ◽  
Release Studies ◽  
Franz Diffusion Cells ◽  
Physical And Chemical ◽  
Gel Formulations ◽  
Vitro Release

Objective: The purpose of the recent study was to formulate glibenclamide gels for transdermal drug release, and to evaluate the oleic acid effect on the release of the preparations. Methods: Oleic acid was used at a range of concentrations in the gel formulations and its effects observed in Glibenclamide gel using In vitro release of drug was done in Franz diffusion cells, whereas pH 7.4 Phosphate buffer was used for release studies. Formulations were characterized by clarity, pH, homogeneity, viscosity, spreadabilty, skin irritation, drug content, stability studies. Scanning calroimetry analysis (SCA) and XRD studies were performed to assess the physical and chemical interactions. Results: Release profiles in vitro were observed. The released quantity of drug recovered from the glibenclamide gel after the addition of 1% oleic acid, increased with increasing concentration of the enhancer that is oleic acid. Whereas drug quantity recovered in the receptor solvent was 69.999% of Glibenclamide gel having 3% oleic acid. All the formulation were physicochemically stable. The data was statistically analyzed by using SPSS and DD solver. Conclusion: The drug is released and the oleic acid does enhance the release of the drug with the increase in its concentration.

scholarly journals Formulation of Creams Containing Spirulina Platensis Powder with Different Nonionic Surfactants for the Treatment of Acne Vulgaris

Molecules ◽  
2020 ◽  
Vol 25 (20) ◽  
pp. 4856
Author(s):  
Liza Józsa ◽  
Zoltán Ujhelyi ◽  
Gábor Vasvári ◽  
Dávid Sinka ◽  
Dániel Nemes ◽  
...  
Keyword(s):  
Spirulina Platensis ◽  
Nonionic Surfactants ◽  
Acne Vulgaris ◽  
Diffusion Method ◽  
Radical Scavenger ◽  
Promising Alternative ◽  
Radical Scavenger Activity ◽  
Scavenger Activity ◽  
Broth Microdilution Method

Natural products used in the treatment of acne vulgaris may be promising alternative therapies with fewer side effects and without antibiotic resistance. The objective of this study was to formulate creams containing Spirulina (Arthrospira) platensis to be used in acne therapy. Spirulina platensis belongs to the group of micro algae and contains valuable active ingredients. The aim was to select the appropriate nonionic surfactants for the formulations in order to enhance the diffusion of the active substance and to certify the antioxidant and antibacterial activity of Spirulina platensis-containing creams. Lyophilized Spirulina platensis powder (SPP) was dissolved in Transcutol HP (TC) and different types of nonionic surfactants (Polysorbate 60 (P60), Cremophor A6:A25 (CR) (1:1), Tefose 63 (TFS), or sucrose ester SP 70 (SP70)) were incorporated in creams as emulsifying agents. The drug release was evaluated by the Franz diffusion method and biocompatibility was tested on HaCaT cells. In vitro antioxidant assays were also performed, and superoxide dismutase (SOD) and 2,2-diphenyl-1-picrylhydrazyl (DPPH) assays were executed. Antimicrobial activities of the selected compositions were checked against Staphylococcus aureus (S. aureus) and Cutibacteriumacnes (C. acnes) (formerly Propionibacterium acnes) with the broth microdilution method. Formulations containing SP 70 surfactant with TC showed the most favorable dissolution profiles and were found to be nontoxic. This composition also showed significant increase in free radical scavenger activity compared to the blank sample and the highest SOD enzyme activity was also detected after treatment with the cream samples. In antibacterial studies, significant differences were observed between the treated and control groups after an incubation time of 6 h.

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