Development of a Synthetic Surfactant Using a Surfactant Protein-C Peptide Analog: In Vitro Studies of Surface Physical Properties

Chong-Woo Bae; Sung-Hoon Chung; Yong-Sung Choi

doi:10.3349/ymj.2016.57.1.203

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This article has been corrected. See "Erratum to “Development of a Synthetic Surfactant Using a Surfactant Protein-C Peptide Analog: In Vitro Studies of Surface Physical Properties” by Bae CW, et al. (Yonsei Med J 2016;57(1):203–208.)" in Volume 61 on page 110.

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Bae, Chung, and Choi: Development of a Synthetic Surfactant Using a Surfactant Protein-C Peptide Analog: In Vitro Studies of Surface Physical Properties

Original Article

Pulmonology

Yonsei Medical Journal 2016; 57(1): 203-208.

Published online: 30 November 2015

DOI: https://doi.org/10.3349/ymj.2016.57.1.203

Development of a Synthetic Surfactant Using a Surfactant Protein-C Peptide Analog: In Vitro Studies of Surface Physical Properties

Chong-Woo Bae, Sung-Hoon Chung, Yong-Sung Choi

Department of Pediatrics, Kyung Hee University School of Medicine, Seoul, Korea.

Corresponding author: Dr. Chong-Woo Bae, Department of Pediatrics, Kyung Hee University Hospital at Gangdong, 892 Dongnam-ro, Gangdong-gu, Seoul 05278, Korea. Tel: 82-2-440-6130, Fax: 82-2-440-7175, baecw@khnmc.or.kr

Received 1 April 2015 Revised 1 September 2015 Accepted 1 October 2015

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Purpose

Pulmonary surfactant (PS) replacement has been the gold standard therapy for neonatal respiratory distress syndrome; however, almost all commercial PSs contain animal proteins. We prepared a synthetic PS by using a human surfactant protein (SP) analog and evaluated its in vitro properties.

Materials and Methods

A peptide sequence (CPVHLKRLLLLLLLLLLLLLLLL) of human SP-C was chosen to develop the peptide analog (SPa-C). The new synthetic SP-C PS (sSP-C PS) was synthesized from SPa-C, dipalmitoyl phosphatidylcholine, phosphatidyl glycerol, and palmitic acid. Physical properties of the sSP-C PS were evaluated by measuring the maximum and minimum surface tensions (STs), surfactant spreading, and adsorption rate. In addition, we recorded an ST-area diagram. The data obtained on sSP-C PS were subsequently compared with those of purified natural bovine surfactant (PNBS), and the commercial product, Surfacten®.

Results

The sSP-C PS and Surfacten® were found to have maximum ST values of 32-33 mN/m, whereas that of PNBS was much lower at 19 mN/m. The minimum ST values of all three products were less than 10 mN/m. The values that were measured for the equilibrium ST of rapidly spreading sSP-C PS, Surfacten®, and PNBS were 27, 27, and 24 mN/m, respectively. The surface adsorptions were found to be the same for all three PSs (20 mN/m). ST-area diagrams of sSP-C PS and Surfacten® revealed similar properties.

Conclusion

In an in vitro experiment, the physical properties exhibited by sSP-C PS were similar to those of Surfacten®. Further study is required to evaluate the in vivo efficacy.

Keywords: Pulmonary surfactant, surfactant protein-C, synthetic peptide syntheses, respiratory distress syndrome, surface tension

INTRODUCTION

Respiratory distress syndrome (RDS) is a disease of pulmonary surfactant (PS) deficiency in newborn babies, particularly preterm infants. Although recent treatments for RDS have accomplished markedly improved outcomes, RDS remains a major cause of death among newborn babies. PS is a phospholipidprotein complex that functions in the human lung to maintain alveolar patency. Since the introduction and use of artificial PS for RDS treatment, the survival rate of preterm infants has improved markedly.1 2 3 This evolutionary change in both therapy and prognosis has been observed over the past two decades in Korea.4 5 6 7 8 9

Most of the commercially used artificial PSs are derived from animal (cow or pig) lung tissue. These animal-derived PSs contain surfactant protein (SP) from animal lung extracts, a point that raises several worrisome questions. Such PSs contain animal antigenicity, which might have potential infectious burden. Additionally, the slaughter of a large number of cows or pigs is needed to produce commercial vials, leading to increased production costs. Thus, there exists a need to produce artificial PS via completely synthetic methods without animal protein components. Lucinactant (Surfaxin®), which contains synthesized KLLLL peptide mimicking human SP-B, was developed and approved by the Food and Drug Administration in 2012.10 Recombinant SP-C based surfactant, Venticute® was also developed; however, clinical trials have been withheld.11 12 Additionally, in vitro and animal studies using synthetic analogues, such as Mini-B and CHF5633 (Chiesi Farmaceutici S.p., Parma, Italy), have recently been published.13 14

The authors conducted a synthetic peptide SP-C analogue-based surfactant study. We selected the peptide sequence CP VHLKRLLLLLLLLLLLLLLLL [SP-CL16(6-28)] for the SP-C analog using the methods of Otsubo, et al.15 We added several artificial phospholipids to prepare synthetic SP-C pulmonary surfactant (sSP-C PS). This preliminary study is the first step of our effort to determine the optimal composition with SP-CL16(6-28), for example, adding SP-B analog in the next step. Our eventual goal is to develop complete synthetic artificial surfactant and to conduct a clinical trial in the future. However, we first conducted an in vitro study to determine the physical properties of sSP-C PS prior to conducting an in vivo study with different compositions. Control subjects included purified natural bovine surfactant (PNBS)16 and a commercial product, Surfacten®, which contains bovine SPs.17 Pulsating bubble surfactometer and modified Wilhelmy balance tests were used to measure surface tension. By comparing these three groups, we evaluated the physical efficacy of sSP-C PS in vitro to assess the possibility of a next-generation synthetic surfactant.

MATERIALS AND METHODS

Preparation of sSP-C PS and PNBS

The sequence of CPVHLKRLLLLLLLLLLLLLLLL was chosen to prepare the SP-C peptide analog.15 The synthesized peptide was obtained from Anygen Co., Ltd. (Jangseong, Korea). As PS is composed mostly of phospholipids, we used dipalmitoyl phosphatidylcholine (DPPC, Sigma-Aldrich Corp., St. Louis, MO, USA), phosphatidylglycerol (PG, Sigma-Aldrich Corp., St. Louis, MO, USA), and palmitic acid (PA, Sigma-Aldrich Corp., St. Louis, MO, USA). We mixed DPPC, PG, PA, and SP-C 75:25:10:3 (w/w) and lyophilized the mixture to obtain sSP-C PS powder.18 To obtain PNBS, intact lungs of healthy cows were extracted. Normal saline (37℃) was instilled via the airway and re-suctioned after several rounds of gentle massage. Twenty liters of normal saline was used for each pair of lungs (approximately 5 kg). The obtained fluid was centrifuged at 500 g for 10 min to remove tissue remnants and blood cells. Then, a 15000 g centrifuge was applied over 60 min at 4℃ to obtain a PS pellet. To purify this crude natural surfactant (CNS), 4-5 mL of CNS pellet was diluted in 0.9% saline to be 30 mL of emulsion, and 48 mL of 26% sodium bromide solution was added. This was centrifuged at 24000 rpm for 120 minutes. In the middle, a white thin layer was obtained and mixed with normal saline. The pellet after 10 minutes of 500 g centrifugation was obtained and used as PNBS.16 19 20

Measurement of surface physical properties of sSP-C PS

A pulsating bubble surfactometer was used to measure surface tension (ST), specifically maximum and minimum ST. Modified Wilhelmy balance equipment was used to measure surface spreading rate and surface adsorption rate and to obtain an ST-area diagram. The surface spreading rate was defined as the time needed for surfactant particles to reach equilibrium ST when the PSs were placed on the fluid surface. We subsequently measured the equilibrium ST. The surface adsorption rate was defined as the time required for PSs to reach equilibrium ST within one minute of being placed under the fluid surface and rising to the surface. We measured the equilibrium ST thereafter as well.

Analysis of the surface physical properties

The measured values of the three different groups (sSP-C PS, Surfacten®, and PNBS) were compared with each other. The ideal PS physical properties included a minimum ST of less than 10 mN/m and a maximum ST of 30 mN/m measured using the pulsating bubble surfactometer and fulfilled Fujiwara's criteria based on the modified Wilhelmy balance test.21 The criteria were as follows: 1) rapid surface spreading (less than 10 seconds to reach an equilibrium ST of 24-27 mN/m), 2) rapid surface adsorption (less than one minute to reach an equilibrium ST of 27-30 mN/m), 3) a minimum ST of less than 10 mN/m with only 20-30% surface compression area, 4) a maximum ST of 27-30 mN/m with 100% surface compression area off, and 5) very low surface compressibility (less than 0.03 cm/dyne at ST 10 mN/m).

RESULTS

Minimum and maximum ST measured using pulsating bubble surfactometer

Minimum and maximum ST values measured using the pulsating bubble surfactometer are depicted in Table 1. All minimum STs measured at five minutes were less than 10 mN/m; however, the maximum STs at five minutes exhibited a different pattern. sSP-C PS and Surfacten® showed similar maximum ST values of 32-33 mN/m, and PNBS showed a maximum ST of only 18-19 mN/m.

Surface spreading rate, adsorption rate, and ST-area diagram using the modified Wilhelmy balance test

Results rendered from the modified Wilhelmy balance test are depicted in Fig. 1 and Table 2. The equilibrium STs measured immediately after rapid spreading (within 10 seconds) were 27.0 mN/m (sSP-C SP), 27.0 mN/m (Surfacten®), and 24 mN/m (PNBS), suggesting that all three preparations exhibit an effective surfactant physical property. The equilibrium STs measured immediately after rapid adsorption (within one minute) for sSP-C PS and Surfacten® were both 30.0 mN/m, an effective physical property; however, that of PNBS was 31 mN/m, which was relatively ineffective. Minimum STs in the ST-area diagrams were 8.0 mN/m (sSP-C PS, effective), 6.0 mN/m (Surfacten®, effective), and 14 mN/m (PNBS, ineffective). Maximum STs were 39 mN/m (sSP-C PS, ineffective), 28.0 mN/m (Surfacten®, effective), and 27 mN/m (PNBS, effective). Surface compressibility values at 10 mN/m ST were 0.03 cm/dyne (sSP-C PS, effective), 0.03 cm/dyne (Surfacten®, effective), and 0.05 cm/dyne (PNBS, ineffective).

DISCUSSION

Human PS is a complex consisting of 86% phospholipids, 8% neutral lipids, and 6% SP. DPPC (50%) and PG (8%) are the most important phospholipids for the surface activity of PS. PS has four main surfactant proteins, SP-A, B, C, and D. Hydrophilic SP-A and D are removed in the manufacturing process; thus, current animal-derived PSs that are clinically used to treat neonatal RDS contain only hydrophobic SP-B and C. Therefore, we considered using SP-B alone, SP-C alone, or a mixture of both as SP in the production of a next-generation artificial PS. We prepared synthetic artificial PS (sSP-C PS) using a synthetic peptide SP-C analogue and conducted an in vitro study to assess the surface physical properties of sSP-C PS as a first step toward deciding whether it should be used alone or as a mixture with SP-B for artificial PS.

Based on the "ideal standard surface properties of artificial PS in vitro study,"21 results comparing sSP-C PS with Surfacten® and PNBS are depicted in Table 2, and the analysis of the current study may be summarized as follows. sSP-C PS and Surfacten® exhibited similar properties, as shown by the modified Wilhelmy balance test, with the exception of maximum ST. They also showed similar properties, including maximum ST, based on the pulsating bubble surfactometer test. These results suggest that sSP-C PS and Surfacten® have similar surface physical properties. PNBS differed from Surfacten®, exhibiting a minimum ST of more than 10 mN/m on both the modified Wilhelmy balance test and the pulsating bubble surfactometer test. Additionally, PNBS showed a surface compressibility of more than 0.03 at an ST of 10 mN/m on the modified Wilhelmy balance test. This finding is consistent with that when the phospholipids were added to PBNS in order to readjust components in preparation for Surfacten®. These results suggest that sSP-C PS, the subject of this study, can be used as an artificial PS that is comparable to commercialized Surfacten®.

Bovine surfactants (Surfacten®, Survanta®, Infasurf®, Alveofact®, Newfactan®) and porcine surfactants (Curosurf®), which have all been clinically proven to be effective, are used worldwide.1 2 3 22 23 24 25 26 27 According to a recent search in the Cochrane database of systematic reviews of several meta-analyses of these agents, the overall relative risk of mortality was decreased when the following procedures were observed with such agents: 1) administration of multiple doses rather than a single dose, 0.63; 2) use of animal-derived surfactant rather than synthetic surfactants, 0.86; 3) prophylactic rather than selective use, 0.61; 4) early rather than delayed selective treatment, 0.87; and 5) use of the INSURE (INtubation SURfactant Extubation) technique rather than surfactant administration followed by continued mechanical ventilation, 0.38 in preterm newborns with RDS.2 28 29 30 31 Exogenous surfactants also decreased neonatal mortality and neonatal pneumothorax by 50% and improved overall infant mortality by 6% in the United States.3 Artificial PS preparations are becoming a popular method for early prophylactic or therapeutic treatment of neonatal RDS.

However, concerns about the immunogenicity of animalderived PSs and bovine prion infection have not been clearly addressed. For this reason, human-derived PS preparations are needed. Creating artificial PS with the same structures as human PS is merely a starting point for developing human-derived PS preparations for the next generation. There exist only a small number of studies on this topic.

The progress summary for the development of synthetic surfactants is depicted in Table 3.32 33 Among these, Lucinactant (Surfaxin®) made with the KL4 peptide of SP-B was approved by the FDA in 2012.10 Development of Venticute®, a gene recombinant SP-C (rSP-C0), was stopped during clinical trials.11 12 rSP-C surfactant improved lung function in animal models; however, treatment with Venticute® in patients with acute respiratory distress syndrome (ARDS) did not improve survival, despite having a positive effect on gas exchange.34 35 Further clinical trial using Venticute® is no longer in progress; however, the ARDS trial was notably limited, as the population included only adult patients and not infants with RDS. Therefore, it is worthwhile for many researchers to continue studies regarding various combinations of synthetic analogs and phospholipid profiles. More studies are in progress as shown in Table 3; however, clinical outcomes of these synthetic surfactants are not currently being measured.

Human SP-C consists of 35 amino acids and has an α helical structure, which is extremely hydrophobic.36 Johansson, et al.37 stressed that the poly-Val structure of synthetic SP-C attenuated the α helix unlike the native SP-C and eventually lowered surface activity. From this perspective, Nilsson, et al.38 substituted poly-Val with poly-Leu, which showed good surface activity with an α helical structure comparable to that of native SP-C. Therefore, it is beneficial to use poly-Leu instead of poly-Val when synthesizing SP-C peptide. Interestingly, Takei, et al.39 shortened the C terminal length while maintaining the poly-Leu sequence and tested several poly-Leu SP-C analog peptides. Notably, SP-CL16(6-28) showed the best biophysical activity, and this was used in our experiment (SP-C analog peptide, CPVHLKRLLLLLLLLLLLLLLLL). Otsubo and Takei40 tested various phospholipids mixed with SP-CL16(6-28) and suggested that palmitoyl-oleoyl PG (POPG) should be used instead of egg PG, as POPG consists of a single compound. In our study, we agreed with the choice of the CPVHLKRLLLLLL LLLLLLLLLL sequence; however, we nevertheless decided to use egg PG. Our results confirmed that the present sequence has good surface activity, based on the comparison with PNBS as well as Surfacten®. PNBS is a natural extract that is not used for limited clinical utility. Fujiwara, et al.17 41 developed effective preparations of Surfacten® by readjusting PNBS and adding phospholipids. In our study, PNBS also showed no significant effect.

In conclusion, the synthetic peptide SP-C analogue was mixed with DPPC, PG, PA, and SP-C (75:25:10:3, w/w) and lyophilized. It showed surface physical properties that were comparable to those of the current commercially used Surfacten®. This suggests that sSP-C PS, the subject of this study, can be used as an artificial PS and is equivalent to commercialized Surfacten®. The main limitation of this study was that it was an in vitro study and was not tested in vivo with animals. To validate our findings, pressure-volume curves and histologic percentages of alveolar areas would need to be measured using rabbit fetal RDS models by administering sSP-C PS in vivo. In this study, we present the results of the in vitro study in advance. We are planning to begin the next step of our research by assessing the properties of the preparation using SP-B alone and using a mixture of SP-B and SP-C.

Figures and Tables

Fig. 1

Physical property diagrams of the three different preparations. (A) The graph shows the surface spreading rate. The equilibrium surface tension measurements obtained within 10 seconds were similar to those of Surfacten® and the synthetic surfactant protein C pulmonary surfactant (sSP-C PS); however, a lower value was obtained with purified natural bovine surfactant (PNBS). (B) The graph shows the surface adsorption rate curve. Both Surfacten® and PNBS reached rapid adsorption equilibrium surface tension within one minute, while sSP-C PS required more than one minute to reach equilibrium. (C) The graph shows the surface tension-area diagram. All three surfactant preparations exhibited reproducible hysteresis curves.

Table 1

Comparison of Minimum and Maximum STs of Three Pulmonary Surfactant Preparations Measured Using a Pulsating Bubble Surfactometer

	Minimum ST (mN/m)		Maximum ST (mN/m)
	1 min	5 min	1 min	5 min
sSP-C PS (n=10)	8.5±0.9	7.7±0.8	33.8±2.5	33.9±2.4
Surfacten® (n=10)	6.4±0.7	5.7±0.6	33.2±1.7	32.5±1.4
PNBS (n=10)	10.2±1.2	8.3±1.3	18.6±2.2	19.0±1.8

sSP-C PS, synthetic surfactant protein C pulmonary surfactant; ST, surface tension; PNBS, purified natural bovine surfactant.

Table 2

Comparison of Findings of Three Surfactant Preparations Measured Using a Modified Wilhelmy Balance

	sSP-C PS	Surfacten®	PNBS
Rapid surface spreading (less than 10 sec to reach an equilibrium ST of 24-27 mN/m) (mN/m)	27.0 (effective)	27.0 (effective)	24.0 (effective)
Rapid surface adsorption (less than 1 min to reach a equilibrium ST of 27-30 mN/m) (mN/m)	30.0 (effective)	30.0 (effective)	31.0 (ineffective)
Minimum ST less than 10 mN/m with only 20-30% surface compression (mN/m)	8.0 (effective)	6.0 (effective)	14.0 (ineffective)
Reproducible ST-area diagram with maximum ST of 27-30 mN/m (mN/m)	39.0 (ineffective)	28.0 (effective)	27.0 (effective)
Very low surface compressibility of less than 0.03 cm/dyne at ST 10 mN/m (cm/dyne)	0.03 (effective)	0.03 (effective)	0.05 (ineffective)

sSP-C PS, synthetic surfactant protein C pulmonary surfactant; ST, surface tension; PNBS, purified natural bovine surfactant.

Table 3

Classification of Synthetic Surfactants Based on Peptide Content

Based on simplified peptides

WMAP10

KL4

KL4-surfactant (Surfaxin)

Poly-N-substituted glycines (peptides) with α-chiral side chains

Based on surfactant protein-B analogs

Peptides that cover the C-terminal partus

Peptides that cover the N-terminal partus

dSP-B1-25

Mini-B

Based on SP-C analogs

Synthetic SP-C analogs with native poly-Val sequence

Poly-Val àpoly-Leu-substituted SP-C analog [SP-C(Leu)]

SP-C (LKS)

SP-C33

SP-C30

Modified from Curstedt T, Johansson, J. Biol Neonate 2005;87:332-7,33 and Kim YD. J Korean Soc Neonatol 2012;19:184-94.32

ACKNOWLEDGEMENTS

This work was supported by the Kyung Hee University research fund (20110897).

Notes

The authors have no financial conflicts of interest.

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