Transdermal drug delivery is an alternative to oral or invasive drug delivery systems. This approach is associated with several advantages including its ability to bypass first-pass metabolism and its non-invasive delivery of drugs that can lead to better patient compliance.
Study: Non-invasive transdermal delivery of biomacromolecules with fluorocarbon-modified chitosan for melanoma immunotherapy and transdermal vaccines. Image Credit: Volodimir Zozulinskyi / Shutterstock.com
Despite its advantages, transdermal drug delivery is limited to drugs that are strongly hydrophobic with lower molecular mass. Thus, hydrophilic macromolecules like peptides, nucleic acids, and proteins cannot be efficiently delivered by this approach. Transdermal delivery systems for anti-severe acute respiratory syndrome coronavirus 2 (anti-SARS-CoV-2) vaccines are a current area of research.
Several transdermal drug delivery systems have been developed for bio-macromolecules like proteins. However, these systems are associated with several challenges including unsatisfactory efficiency, inability to deliver high molecular weight proteins, and other unwanted effects such as skin damage leading to infections, inability to self-dispense, and complicated manufacturing processes.
A biodegradable natural cationic polymer known as chitosan (CS) possesses mucoadhesive and antibiotic properties. In particular, fluorocarbon modified CS (FCS) has demonstrated efficient transmucosal delivery of drugs, which led researchers in a recent Research Square* preprint to assess the efficacy of this system for the development of SARS-CoV-2 vaccines and tumor immunotherapy. The paper is under consideration in Nature Portfolio Journal.
In the current study, nanocomplexes were formed by mixing FCS with ovalbumin (OVA) and immunoglobulin G (IgG) to create FCS/IgG and FCS/OVA, respectively. The structure and activity of IgG and OVA remained nearly unchanged after forming nanocomplexes with FCS.
The transdermal delivery of the FCS/IgG and FCS/OVA were confirmed. Both the nanocomplexes showed highest penetration ability in the skin at a 1:1 mass ratio.
The mechanisms underlying the intercellular transdermal delivery of these nanoparticles were studied by using a monolayer of human skin dermis HACAT cells, wherein the researchers monitored the transepithelial electrical resistance (TEER) across its two sides. The addition of FCS/IgG temporarily opened the tight junctions and enlarged the intercellular spaces.
The researchers then assessed the transappendageal route of transdermal drug delivery, which is important in the transport of water-soluble macromolecules across sebaceous glands, hair follicles, and sweat glands. This route was found to play an essential role in the transdermal delivery of FCS-based nanoparticles.
Similarly, the researchers also investigated the transcellular route of transdermal drug delivery, which reflects direct drug passage across keratinocytes. A negligible involvement of the transcellular route was found in the transdermal delivery of FCS-based nanoparticles. Thus, it was inferred that the transappendageal and intercellular routes were the main transdermal drug delivery systems of the FCS-containing nanoparticles.
An ‘antibody FCS complex/radioisotope125 labeled IgG (125I-IgG) or FCS/125 I-IgG cream formulation was topically applied on mice melanoma tumors to quantify transmitted antibodies at different time intervals. A continuous transmission and even distribution of antibodies in the tumor was observed.
Thereafter, an live treatment of the melanoma tumors by transdermal delivery of FCS/anti-programmed death ligand-1 (FCS/aPDL 1) was conducted. Mice with melanoma tumors were divided into four categories including untreated, treated with intravenous delivery of free aPDL1, as well as those treated with cream-based transdermal delivery of CS/PDL1. All mice were observed for twenty days.
The FCS/aPDL1 treated group achieved successful tumor inhibition after the third treatment with the longest survival and lowest tumor growth rates. However, negligible tumor inhibition was elicited by the free aPDL1 and CS/aPDL1 treated groups.
To study the immune activation mechanism of transdermally delivered immunotherapy, tumors from different groups were collected and analyzed on day 12. The FCS/aPDL treated group revealed an increased percentage of CD4+ and CD8+ T-cells.
Transdermal delivery of SARS-CoV-2 vaccine. (a) A schematic illustration for transdermal delivery of SARS-CoV-2 vaccine and the triggered immune responses. After transdermal delivery, such SARS-CoV-2 nano-vaccines could activate immune cells such as DCs in the dermis, or migrate to the nearby lymph nodes for immune activation. (b) Schematic illustration of the experimental design showing transdermal delivery of SARS-CoV-2 vaccine. (c&d) DLS (c) and zeta potential (d) of FCS-based transdermal vaccines with different mass ratios from 1:1:1 to 4:1:1. (e) The skin penetration ability of FCS-based transdermal vaccine with different mass ratios. (f) SARS-CoV-2 specific IgG antibody titers at different time intervals determined by ELISA. (g&h) Quantification of CD4+ T cells, CD8+ T cells in the spleen at day 28. (i&j) Quantification of IFN-γ+ CD4 secrecy+ T cells (CD3+CD4+ IFN-γ+) and CD8+ T cells (CD3+CD8+ IFN-γ+) in the spleen at day 28. (k&l) Quantification of OVA-Cy5.5+ (CD45+CD11c+Cy5.5+) in DCs in (k) lymph nodes and (l) skin. (m&n) Quantification of (m) DC maturation (CD45+CD11c+CD86+) and (n) T cell receptor (TCR) activation (CD45+CD3+CD8+CD69+) in lymph nodes. All illustrations were created with BioRender.com. Data are presented as mean ± standard deviation (n=4 or 6). Statistical significance was calculated via one-way ANOVA with a Tukey post-hoc test. *P < 0.05; **P<0.01; ***P < 0.001.
The CD8+ T-cell activity was analyzed using granzyme B, Ki67, and interferon g (IFN-g). An effective infiltration and activation of T-cells marked by elevated levels of all three markers were found in the FCS/aPDL treated group.
Infiltration of CD4+ and CD8+ T-cells, as well as the expression of the three aforementioned biomarkers, remained unchanged in mice treated with IV aPDL1 and transdermal CS/aPDL1 transdermal. It was thus inferred that transdermally delivered FCS/aPDL resulted in an increased antitumor immune response.
A combination therapy using anti-cytotoxic T-lymphocyte-associated protein 4 (aCTLA4) and aPDL1 together with FCS-based transdermal delivery was assessed. The transdermal delivery exhibited a synergistic therapeutic effect of FCS/ aPDL1/ACTLA4 as compared to the transdermally delivered FCS/aPDL1 or FCS/ACTLA4.
Interestingly, the combined therapy inhibited distant tumors as well. Upon analysis of the distant tumors, an increase in CD8+ T-cells, particularly Ki67+ CD8+ T-cells, together with decreased regulatory T-cells (Tregs), were found.
Next, FCS-based transdermal SARS-CoV-2 vaccine was synthesized (FCS/S1/PolyIC). OVA was used as an antigen, with the FCS:antigen:PolyIC ratio optimized in the vaccine. FCS/OVA/PolyIC at a 2:1:1 mass ratio with a relatively small size revealed the highest skin penetrability and was further studied.
In-vivo experiments were conducted by dividing mice into three groups of untreated, treated with transdermally delivered FCS/S1/PolyIC, and treated with subcutaneously injected S1/PolyIC. Both treated groups revealed similar antibody titers after two weeks, thereby indicating a similar B-cell activation. Effective activation of humoral immunity was observed in 30 days.
Cell immunity was assessed by evaluating the spleen of all mice for cytotoxic T-cells 28 days after primeval administration. To this end, CD4+ and CD8+ T-cell infiltration were similar in all groups.
IFN-g secretion by T-cells and the percentage of the memory T-cells was substantially increased in transdermally delivered FCS/S1/PolyIC. This indicates a stronger T-cell response and long-term immune memory effect as compared to the subcutaneously injected S1/PolyIC.
The exact permeation ability of the vaccines was measured using Cy5.5 labeled OVA as antigen by measuring the antigen accumulation in the lymph nodes after 24 hours of vaccine administration. Lower OVA retention was found in mice that received transdermally delivered FCS/S1/PolyIC
The dendritic cells (DCs) beneath the skin revealed higher OVA uptake in FCS/S1/PolyIC treated mice. Thus, transdermal delivery of this vaccine activates DCs directly, which then migrates to lymph nodes triggering further immune responses.
Comparatively, after the subcutaneous injection, the antigen and adjuvant migrate separately to lymph nodes and are more prone to depletion by non-specific immune cells, thus indicating a less efficient activation of DCs.
Comparable T-cell activation and DC maturation were observed with both routes of vaccine administration. It was thus inferred that FCS-based transdermal vaccine delivery triggers stronger cell immunity and similar humoral immunity but an inferior antigen penetration as compared to the subcutaneous vaccine administration.
Taken together, the current study demonstrates that the FCS-based transdermal delivery system is efficient in delivering biomacromolecules, which expands the potential range of topically administered therapeutics.
Research Square publishes preliminary scientific reports that are not peer-reviewed and, therefore, should not be regarded as conclusive, guide clinical practice/health-related behavior, or treated as established information.