Novel SmartReservoirs for hydrogel-forming microneedles to improve the transdermal delivery of rifampicin

被引:11
作者
Abraham, Abraham M. [1 ]
Anjani, Qonita Kurnia [1 ]
Adhami, Masoud [1 ]
Hutton, Aaron R. J. [1 ]
Larraneta, Eneko [1 ]
Donnelly, Ryan F. [1 ]
机构
[1] Queens Univ Belfast, Med Biol Ctr, Sch Pharm, 97 Lisburn Rd, Belfast BT9 7BL, North Ireland
关键词
SKIN INFECTIONS; DRUG-DELIVERY; IN-VITRO; ETHOSOMES; RISK;
D O I
10.1039/d4tb00110a
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Hydrogel-forming microneedles (HF-MNs) are composed of unique cross-linked polymers that are devoid of the active pharmaceutical ingredient (API) within the microneedle array. Instead, the API is housed in a reservoir affixed on the top of the baseplate of the HF-MNs. To date, various types of drug-reservoirs and multiple solubility-enhancing approaches have been employed to deliver hydrophobic molecules combined with HF-MNs. These strategies are not without drawbacks, as they require multiple manufacturing steps, from solubility enhancement to reservoir production. However, this current study challenges this trend and focuses on the delivery of the hydrophobic antibiotic rifampicin using SmartFilm-technology as a solubility-enhancing strategy. In contrast to previous techniques, smart drug-reservoirs (SmartReservoirs) for hydrophobic compounds can be manufactured using a one step process. In this study, HF-MNs and three different concentrations of rifampicin SmartFilms (SFs) were produced. Following this, both HF-MNs and SFs were fully characterised regarding their physicochemical and mechanical properties, morphology, Raman surface mapping, the interaction with the cellulose matrix and maintenance of the loaded drug in the amorphous form. In addition, their drug loading and transdermal permeation efficacy were studied. The resulting SFs showed that the API was intact inside the cellulose matrix within the SFs, with the majority of the drug in the amorphous state. SFs alone demonstrated no transdermal penetration and less than 20 +/- 4 mu g of rifampicin deposited in the skin layers. In contrast, the transdermal permeation profile using SFs combined with HF-MNs (i.e. SmartReservoirs) demonstrated a 4-fold increase in rifampicin deposition (80 +/- 7 mu g) in the skin layers and a permeation of approx. 500 +/- 22 mu g. Results therefore illustrate that SFs can be viewed as novel drug-reservoirs (i.e. SmartReservoirs) for HF-MNs, achieving highly efficient loading and diffusion properties through the hydrogel matrix. SmartReservoirs (SRs) are novel drug-reservoirs for hydrogel-forming microneedles (HF-MNs). SRs improved rifampicin solubility and diffusion through the HF-matrix, thereby enhancing the transdermal permeation of the poorly soluble antibiotic.
引用
收藏
页码:4375 / 4388
页数:15
相关论文
共 75 条
[1]   SmartFilm Tablets for Improved Oral Delivery of Poorly Soluble Drugs [J].
Abdelkader, Ayat ;
Preis, Eduard ;
Keck, Cornelia M. .
PHARMACEUTICS, 2022, 14 (09)
[2]   Cucumber-Derived Exosome-like Vesicles and PlantCrystals for Improved Dermal Drug Delivery [J].
Abraham, Abraham M. ;
Wiemann, Sabrina ;
Ambreen, Ghazala ;
Zhou, Jenny ;
Engelhardt, Konrad ;
Bruessler, Jana ;
Bakowsky, Udo ;
Li, Shu-Ming ;
Mandic, Robert ;
Pocsfalvi, Gabriella ;
Keck, Cornelia M. .
PHARMACEUTICS, 2022, 14 (03)
[3]   Mechanical properties of polypropylene mesh used in pelvic floor repair [J].
Afonso, J. S. ;
Martins, P. A. L. S. ;
Girao, M. J. B. C. ;
Jorge, R. M. Natal ;
Ferreira, A. J. M. ;
Mascarenhas, T. ;
Fernandes, A. A. ;
Bernardes, J. ;
Baracat, E. C. ;
de Lima, G. Rodrigues ;
Patricio, B. .
INTERNATIONAL UROGYNECOLOGY JOURNAL, 2008, 19 (03) :375-380
[4]   Solid-state characterization of rifampicin samples and its biopharmaceutic relevance [J].
Agrawal, S ;
Ashokraj, Y ;
Bharatam, PV ;
Pillai, O ;
Panchagnula, R .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 22 (2-3) :127-144
[5]   Liposome-loaded polymeric microneedles for enhanced skin deposition of rifampicin [J].
Anjani, Qonita Kurnia ;
Pandya, Anjali K. ;
Demartis, Sara ;
Dominguez-Robles, Juan ;
Moreno-Castellanos, Natalia ;
Li, Huanhuan ;
Gavini, Elisabetta ;
Patravale, Vandana B. ;
Donnelly, Ryan F. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2023, 646
[6]   Inclusion Complexes of Rifampicin with Native and Derivatized Cyclodextrins: In Silico Modeling, Formulation, and Characterization [J].
Anjani, Qonita Kurnia ;
Dominguez-Robles, Juan ;
Utomo, Emilia ;
Font, Maria ;
Martinez-Oharriz, Maria Cristina ;
Permana, Andi Dian ;
Carcamo-Martinez, Alvaro ;
Larraneta, Eneko ;
Donnelly, Ryan F. .
PHARMACEUTICALS, 2022, 15 (01)
[7]   Versatility of hydrogel-forming microneedles in in vitro transdermal delivery of tuberculosis drugs [J].
Anjani, Qonita Kurnia ;
Permana, Andi Dian ;
Carcamo-Martinez, Alvaro ;
Dominguez-Robles, Juan ;
Tekko, Ismaiel A. ;
Larraneta, Eneko ;
Vora, Lalit K. ;
Ramadon, Delly ;
Donnelly, Ryan F. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2021, 158 :294-312
[8]   Design of multifunctional ethosomes for topical fenretinide delivery and breast cancer chemoprevention [J].
Apolinario, Alexsandra Conceicao ;
Hauschke, Leon ;
Nunes, Jessica Ribeiro ;
Lourenco, Felipe Rebello ;
Lopes, Luciana Biagini .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2021, 623
[9]   Towards nanoformulations for skin delivery of poorly soluble API: What does indeed matter? [J].
Apolinario, Alexsandra Conceicao ;
Hauschke, Leon ;
Nunes, Jessica Ribeiro ;
Lopes, Luciana Biagini .
JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2020, 60
[10]   The Threat of Antimicrobial Resistance on the Human Microbiome [J].
Brinkac, Lauren ;
Voorhies, Alexander ;
Gomez, Andres ;
Nelson, Karen E. .
MICROBIAL ECOLOGY, 2017, 74 (04) :1001-1008