Optimization and evaluation of itraconazole-loaded nanostructured lipid carriers incorporated gel for topical drug delivery

Gopa Roy Biswas

Makale detayları

Optimization and evaluation of itraconazole-loaded nanostructured lipid carriers incorporated gel for topical drug delivery

Yazarlar:

Gopa Roy Biswas

Yayıncı:

Marmara University

Ana Başlıklar:

Pharmaceutical Sciences | Pharmaceutical Delivery Technologies

Dergi:

Journal of Research in Pharmacy Vol.28 Issue 2, pp.526-544

Belge Tipi:

Makale

Yayın Tarihi:

6/2025

Belge Dili:

İngilizce

Document ID (Org No.):

2001346206

pISSN:

2630-6344

Anahtar kelimeler:

Özet:

 Nanotechnology is a relatively new technology that creates a lot of possibilities for smart drug manufacturing and delivery techniques. Nanostructured lipid carrier NLC is a significant advantage over the other drug delivery system. NLC-employed gel Nanogel, which is composed of hydrophilic polymer network-based nanoparticles, ranges from 10 nm to 1000 nm. Because of its great loading capacity, high stability, extended contact period, and thus extended therapeutic impact, nanogel has been used in topical administration. In this work, Itraconazole has been chosen as an API. With the use of Central Composite Design, NLC has been prepared with two variables. They are combined with solid lipid and liquid lipid, and with the aid of a surfactant and are stabilized in aqueous dispersion. The Hot homogenization technique was adopted for the preparation of the same. The mixture was homogenized for 20 minutes at a speed of 2000-8000 RPM which was afterwards sonicated . The formed NLCs were incorporated into hydrogel using Carbopol 934 P as a gel-forming agent. Particle size was measured with the help of the Dynamic light scattering DLS method. The results revealed that the particles were in nano range 54nm  488nm. Out of 39 optimized combination found through Design of Expert software, the matched prepared formulation NF 3 was subjected to in vitro drug diffusion study, it was found that drug diffusion from that formulation steadily increased and remained constant after 5 hours. Drug diffusion was almost 89.15 in 7 hours. Following an ex vivo permeation investigation on goat skin of the same , it was seen that the permeation of Itraconazole through goat abdominal skin from the optimized product was around 51.67 in 7 hours.

 Nanotechnology is a relatively new technology that creates a lot of possibilities for smart drug manufacturing and delivery techniques. Nanostructured lipid carrier NLC is a significant advantage over the other drug delivery system. NLC-employed gel Nanogel, which is composed of hydrophilic polymer network-based nanoparticles, ranges from 10 nm to 1000 nm. Because of its great loading capacity, high stability, extended contact period, and thus extended therapeutic impact, nanogel has been used in topical administration. In this work, Itraconazole has been chosen as an API. With the use of Central Composite Design, NLC has been prepared with two variables. They are combined with solid lipid and liquid lipid, and with the aid of a surfactant and are stabilized in aqueous dispersion. The Hot homogenization technique was adopted for the preparation of the same. The mixture was homogenized for 20 minutes at a speed of 2000-8000 RPM which was afterwards sonicated . The formed NLCs were incorporated into hydrogel using Carbopol 934 P as a gel-forming agent. Particle size was measured with the help of the Dynamic light scattering DLS method. The results revealed that the particles were in nano range 54nm  488nm. Out of 39 optimized combination found through Design of Expert software, the matched prepared formulation NF 3 was subjected to in vitro drug diffusion study, it was found that drug diffusion from that formulation steadily increased and remained constant after 5 hours. Drug diffusion was almost 89.15 in 7 hours. Following an ex vivo permeation investigation on goat skin of the same , it was seen that the permeation of Itraconazole through goat abdominal skin from the optimized product was around 51.67 in 7 hours.

 Nanotechnology is a relatively new technology that creates a lot of possibilities for smart drug manufacturing and delivery techniques. Nanostructured lipid carrier NLC is a significant advantage over the other drug delivery system. NLC-employed gel Nanogel, which is composed of hydrophilic polymer network-based nanoparticles, ranges from 10 nm to 1000 nm. Because of its great loading capacity, high stability, extended contact period, and thus extended therapeutic impact, nanogel has been used in topical administration. In this work, Itraconazole has been chosen as an API. With the use of Central Composite Design, NLC has been prepared with two variables. They are combined with solid lipid and liquid lipid, and with the aid of a surfactant and are stabilized in aqueous dispersion. The Hot homogenization technique was adopted for the preparation of the same. The mixture was homogenized for 20 minutes at a speed of 2000-8000 RPM which was afterwards sonicated . The formed NLCs were incorporated into hydrogel using Carbopol 934 P as a gel-forming agent. Particle size was measured with the help of the Dynamic light scattering DLS method. The results revealed that the particles were in nano range 54nm  488nm. Out of 39 optimized combination found through Design of Expert software, the matched prepared formulation NF 3 was subjected to in vitro drug diffusion study, it was found that drug diffusion from that formulation steadily increased and remained constant after 5 hours. Drug diffusion was almost 89.15 in 7 hours. Following an ex vivo permeation investigation on goat skin of the same , it was seen that the permeation of Itraconazole through goat abdominal skin from the optimized product was around 51.67 in 7 hours.

 Nanotechnology is a relatively new technology that creates a lot of possibilities for smart drug manufacturing and delivery techniques. Nanostructured lipid carrier NLC is a significant advantage over the other drug delivery system. NLC-employed gel Nanogel, which is composed of hydrophilic polymer network-based nanoparticles, ranges from 10 nm to 1000 nm. Because of its great loading capacity, high stability, extended contact period, and thus extended therapeutic impact, nanogel has been used in topical administration. In this work, Itraconazole has been chosen as an API. With the use of Central Composite Design, NLC has been prepared with two variables. They are combined with solid lipid and liquid lipid, and with the aid of a surfactant and are stabilized in aqueous dispersion. The Hot homogenization technique was adopted for the preparation of the same. The mixture was homogenized for 20 minutes at a speed of 2000-8000 RPM which was afterwards sonicated . The formed NLCs were incorporated into hydrogel using Carbopol 934 P as a gel-forming agent. Particle size was measured with the help of the Dynamic light scattering DLS method. The results revealed that the particles were in nano range 54nm  488nm. Out of 39 optimized combination found through Design of Expert software, the matched prepared formulation NF 3 was subjected to in vitro drug diffusion study, it was found that drug diffusion from that formulation steadily increased and remained constant after 5 hours. Drug diffusion was almost 89.15 in 7 hours. Following an ex vivo permeation investigation on goat skin of the same , it was seen that the permeation of Itraconazole through goat abdominal skin from the optimized product was around 51.67 in 7 hours.

Makale detayları

Optimization and evaluation of itraconazole-loaded nanostructured lipid carriers incorporated gel for topical drug delivery

Yazarlar:

Gopa Roy Biswas

Yayıncı:

Marmara University

Ana Başlıklar:

Pharmaceutical Sciences | Pharmaceutical Delivery Technologies

Dergi:

Journal of Research in Pharmacy Vol.28 Issue 2, pp.526-544

Belge Tipi:

Makale

Yayın Tarihi:

6/2025

Belge Dili:

İngilizce

Document ID (Org No.):

2001346206

pISSN:

2630-6344

Nanostructured lipid carrier

Topical delivery system

Hot homogenization

Nanogel

DLS

In vitro drug diffusion

Permeation

Sayı

Makale detayları

Yazarlar: Gopa Roy Biswas

Yayıncı: Marmara University

Ana Başlıklar: Pharmaceutical Sciences | Pharmaceutical Delivery Technologies

Dergi: Journal of Research in Pharmacy Vol.28 Issue 2, pp.526-544

Belge Tipi: Makale

Yayın Tarihi: 6/2025

Belge Dili: İngilizce

Document ID (Org No.): 2001346206

pISSN: 2630-6344

Sayı

Yazarlar:

Gopa Roy Biswas

Yayıncı:

Marmara University

Ana Başlıklar:

Pharmaceutical Sciences | Pharmaceutical Delivery Technologies

Dergi:

Journal of Research in Pharmacy Vol.28 Issue 2, pp.526-544

Belge Tipi:

Makale

Yayın Tarihi:

6/2025

Belge Dili:

İngilizce

Document ID (Org No.):

2001346206

pISSN:

2630-6344